The meaning of Sutphin
Americanized form of Dutch Van Zutphen: habitational name for someone from Zutphen in the province of Gelderland. Compare Sutfin and Sutphen.
Dictionary of American Family Names, 2nd edition, © Oxford University Press, 2022.
How common is the last name Sutphin in the United States?
According to the Decennial U.S. Census data, the popularity of the surname Sutphin has seen a slight decline between 2000 and 2010. In 2000, Sutphin ranked at 7320 in terms of its prevalence among U.S. surnames but dropped by approximately 8% to a rank of 7904 in 2010. The count of individuals with the surname Sutphin also decreased marginally during this period from 4193 to 4188, representing a change of -0.12%. The proportion of people with the Sutphin surname per 100,000 also reduced by 8.39%, shifting down from 1.55 to 1.42.
2000 | 2010 | Change | |
---|---|---|---|
Rank | #7,320 | #7,904 | -7.98% |
Count | 4,193 | 4,188 | -0.12% |
Proportion per 100k | 1.55 | 1.42 | -8.39% |
Race and Ethnicity of people with the last name Sutphin
On the ethnicity front, the Decennial U.S. Census data shows a minor shift in the ethnic identity associated with the surname Sutphin. The proportion of White individuals bearing the surname decreased slightly from 95.06% in 2000 to 94.51% in 2010. The representation of Asian/Pacific Islander and American Indian and Alaskan Native ethnicities was recorded as zero in 2010, while the 2000 figures were suppressed for privacy (S). The Hispanic representation saw an increase from 1.10% in 2000 to 1.60% in 2010. There was also a small rise in the number of individuals identifying with two or more races under the Sutphin surname, from 0.91% to 1.27%. Conversely, the Black representation saw a decrease, moving from 2.07% in 2000 to 1.98% in 2010.
2000 | 2010 | Change | |
---|---|---|---|
White | 95.06% | 94.51% | -0.58% |
Black | 2.07% | 1.98% | -4.35% |
Hispanic | 1.1% | 1.6% | 45.45% |
Two or More Races | 0.91% | 1.27% | 39.56% |
Asian/Pacific Islander | 0.64% | 0% | 0% |
American Indian and Alaskan Native | 0.21% | 0% | 0% |
Sutphin ancestry composition
23andMe computes an ancestry breakdown for each customer. People may have ancestry from just one population or they may have ancestry from several populations. The most commonly-observed ancestry found in people with the surname Sutphin is British & Irish, which comprises 59.3% of all ancestry found in people with the surname. The next two most common ancestries are French & German (26.6%) and Eastern European (4.4%). Additional ancestries include Italian, Scandinavian, Indigenous American, Spanish & Portuguese, and Ashkenazi Jewish.
Ready to learn more about your ancestry? Get the most comprehensive ancestry breakdown on the market by taking our DNA test. Shop 23andMe
ANCESTRY BREAKDOWN | COMPOSITION |
---|---|
British & Irish | 59.3% |
French & German | 26.6% |
Eastern European | 4.4% |
Other | 9.7% |
Possible origins of the surname Sutphin
Your DNA provides clues about where your recent ancestors may have lived. Having many distant relatives in the same location suggests that you may all share common ancestry there. Locations with many distant relatives can also be places where people have migrated recently, such as large cities. If a large number of individuals who share your surname have distant relatives in a specific area, it could indicate a connection between your surname and that location, stemming from either recent ancestral ties or migration.
Based on 23andMe data, people with last name Sutphin have recent ancestry locations in the United Kingdom of Great Britain and Northern Ireland and Ireland.
RECENT ANCESTRY Location | Percentage |
---|---|
Glasgow City, United Kingdom | 91.50% |
Greater London, United Kingdom | 91.50% |
Merseyside, United Kingdom | 91.50% |
Greater Manchester, United Kingdom | 91.50% |
Belfast, United Kingdom | 91.50% |
What Sutphin haplogroups can tell you
Haplogroups are genetic population groups that share a common ancestor on either your paternal or maternal line. These paternal and maternal haplogroups shed light on your genetic ancestry and help tell the story of your family.
The top paternal haplogroup of people with the surname Sutphin is O-F2415, which is predominantly found among people with East Asian & Indigenous American ancestry. Haplogroup O-F2415 is descended from haplogroup O-M1359. Other common haplogroups include E-M183 and O-F2859, which are predominantly found among people with European and East Asian & Indigenous American ancestry.
The most common maternal haplogroups of people with Sutphin surname are: H1, H, U5a. These most commonly trace back to individuals of European ancestry.
Paternal Haplogroup Origins O-M1359
Your paternal lineage may be linked to the Cham
One of the many populations harboring members of haplogroup O1b1a1a1a1 is the Cham ethnic group, a group of people who speak Austronesian languages in Mainland Southeast Asia. Austronesian languages make up a language family that is extremely large and widespread, comprising over 350 million people on islands such as Madagascar, Easter Island, and many others. However, Austronesian languages are less common on mainland Asia, with a notable exception being the Chamic language. Research suggests that ancestors of the Cham people migrated from Southeast Asian islands to the mainland around the year 500 BCE, and that early Cham populations quickly began mixing with indigenous southern Vietnamese populations. As a result, the Chamic language now has words that were borrowed from languages spoken by indigenous Vietnamese people. It is likely that an ancestral Kinh population was one of the populations that mixed with the Cham people shortly after their migration to mainland Asia.
Your maternal lineage may be linked to Marie Antoinette
Because it is so dominant in the general European population, haplogroup H also appears quite frequently in the continent's royal houses. Marie Antoinette, an Austrian Hapsburg who married into the French royal family, inherited the haplogroup from her maternal ancestors. So did Prince Philip, Duke of Edinburgh, whose recorded genealogy traces his female line to Bavaria. Scientists also discovered that famed 16th century astronomer Nicolaus Copernicus traced his maternal lineages to haplogroup H.
What do people with the surname Sutphin have in common?
Spoiler alert: it's complicated. People with the same last name are usually no more genetically similar than a randomly sampled group of people from the same population. That said, people with the same surname are more likely to have similar ancestries than randomly sampled individuals. The reason is the tendency of people with similar cultural or geographical backgrounds to preferentially mate with one another. That's why people who share a surname may be more likely to share traits and tendencies in common than people within the general population. Check out the percentages below to see the prevalences of tastes, habits, and traits of people with your surname compared with prevalences among 23andMe users.
Preferences
Chocolate Ice Cream
Prefers chocolate flavored ice cream over other flavors.
"Sutphin" Surname 44.4%
23andMe Users 41.3%
Vanilla Ice Cream
Prefers vanilla flavored ice cream over other flavors.
"Sutphin" Surname 30.6%
23andMe Users 36.7%
Like Very Cold Weather
Enjoys weather that is colder than 40 degrees Farenheit
"Sutphin" Surname 34.8%
23andMe Users 24.8%
Likes Hoppy Beer
Like beer that has a strong hop flavor and aroma.
"Sutphin" Surname 23.8%
23andMe Users 20.0%
Likes Boiled Eggs
Likes the taste of hard-boiled eggs.
"Sutphin" Surname 68.8%
23andMe Users 70.2%
Chocolate Ice Cream
Prefers chocolate flavored ice cream over other flavors.
"Sutphin" Surname 44.4%
23andMe Users 41.3%
Vanilla Ice Cream
Prefers vanilla flavored ice cream over other flavors.
"Sutphin" Surname 30.6%
23andMe Users 36.7%
Like Very Cold Weather
Enjoys weather that is colder than 40 degrees Farenheit
"Sutphin" Surname 34.8%
23andMe Users 24.8%
Likes Hoppy Beer
Like beer that has a strong hop flavor and aroma.
"Sutphin" Surname 23.8%
23andMe Users 20.0%
Likes Boiled Eggs
Likes the taste of hard-boiled eggs.
"Sutphin" Surname 68.8%
23andMe Users 70.2%
Chocolate Ice Cream
Prefers chocolate flavored ice cream over other flavors.
"Sutphin" Surname 44.4%
23andMe Users 41.3%
Vanilla Ice Cream
Prefers vanilla flavored ice cream over other flavors.
"Sutphin" Surname 30.6%
23andMe Users 36.7%
Like Very Cold Weather
Enjoys weather that is colder than 40 degrees Farenheit
"Sutphin" Surname 34.8%
23andMe Users 24.8%
Likes Hoppy Beer
Like beer that has a strong hop flavor and aroma.
"Sutphin" Surname 23.8%
23andMe Users 20.0%
Likes Boiled Eggs
Likes the taste of hard-boiled eggs.
"Sutphin" Surname 68.8%
23andMe Users 70.2%
Traits
Misophonia
When sounds made by others, like the sound of chewing or yawning, provoke strong emotional reactions in an individual.
"Sutphin" Surname 33.3%
23andMe Users 27.9%
Cheek Dimples
Small indentations that appear on the cheeks when a person smiles.
"Sutphin" Surname 36.0%
23andMe Users 37.6%
Acrophobia
An intense fear of heights that goes beyond the concern many people feel around significant heights.
"Sutphin" Surname 20.0%
23andMe Users 16.7%
Light Hair
Hair that is blonde or light brown in color
"Sutphin" Surname 75.0%
23andMe Users 50.5%
Straight Hair
Hair with strands that have no visible curl or wave.
"Sutphin" Surname 28.6%
23andMe Users 30.5%
Misophonia
When sounds made by others, like the sound of chewing or yawning, provoke strong emotional reactions in an individual.
"Sutphin" Surname 33.3%
23andMe Users 27.9%
Cheek Dimples
Small indentations that appear on the cheeks when a person smiles.
"Sutphin" Surname 36.0%
23andMe Users 37.6%
Acrophobia
An intense fear of heights that goes beyond the concern many people feel around significant heights.
"Sutphin" Surname 20.0%
23andMe Users 16.7%
Light Hair
Hair that is blonde or light brown in color
"Sutphin" Surname 75.0%
23andMe Users 50.5%
Straight Hair
Hair with strands that have no visible curl or wave.
"Sutphin" Surname 28.6%
23andMe Users 30.5%
Misophonia
When sounds made by others, like the sound of chewing or yawning, provoke strong emotional reactions in an individual.
"Sutphin" Surname 33.3%
23andMe Users 27.9%
Cheek Dimples
Small indentations that appear on the cheeks when a person smiles.
"Sutphin" Surname 36.0%
23andMe Users 37.6%
Acrophobia
An intense fear of heights that goes beyond the concern many people feel around significant heights.
"Sutphin" Surname 20.0%
23andMe Users 16.7%
Light Hair
Hair that is blonde or light brown in color
"Sutphin" Surname 75.0%
23andMe Users 50.5%
Straight Hair
Hair with strands that have no visible curl or wave.
"Sutphin" Surname 28.6%
23andMe Users 30.5%
Habits
Sugary Drink
Drinks one or more sugary drinks per day.
"Sutphin" Surname 35.9%
23andMe Users 21.1%
Vitamin Use
Takes vitamins on a regular basis.
"Sutphin" Surname 45.5%
23andMe Users 45.5%
Kinesthetic Learner
Preferring to learn and process information through hands-on activities, practical experiences, and active engagement.
"Sutphin" Surname 78.3%
23andMe Users 61.5%
Tea Consumption
A preference for drinking caffeinated tea in a particular week.
"Sutphin" Surname 47.6%
23andMe Users 49.2%
Learn Language As Adult
Learning a new language through formal or informal means after 18 years of age.
"Sutphin" Surname 36.0%
23andMe Users 25.8%
Sugary Drink
Drinks one or more sugary drinks per day.
"Sutphin" Surname 35.9%
23andMe Users 21.1%
Vitamin Use
Takes vitamins on a regular basis.
"Sutphin" Surname 45.5%
23andMe Users 45.5%
Kinesthetic Learner
Preferring to learn and process information through hands-on activities, practical experiences, and active engagement.
"Sutphin" Surname 78.3%
23andMe Users 61.5%
Tea Consumption
A preference for drinking caffeinated tea in a particular week.
"Sutphin" Surname 47.6%
23andMe Users 49.2%
Learn Language As Adult
Learning a new language through formal or informal means after 18 years of age.
"Sutphin" Surname 36.0%
23andMe Users 25.8%
Sugary Drink
Drinks one or more sugary drinks per day.
"Sutphin" Surname 35.9%
23andMe Users 21.1%
Vitamin Use
Takes vitamins on a regular basis.
"Sutphin" Surname 45.5%
23andMe Users 45.5%
Kinesthetic Learner
Preferring to learn and process information through hands-on activities, practical experiences, and active engagement.
"Sutphin" Surname 78.3%
23andMe Users 61.5%
Tea Consumption
A preference for drinking caffeinated tea in a particular week.
"Sutphin" Surname 47.6%
23andMe Users 49.2%
Learn Language As Adult
Learning a new language through formal or informal means after 18 years of age.
"Sutphin" Surname 36.0%
23andMe Users 25.8%
Wellness
Migraine
A severe headache characterized by intense pain, sensitivity to light and sound, and often accompanied by nausea and vomiting.
"Sutphin" Surname 21.1%
23andMe Users 16.4%
Cat Allergy
An allergic reaction to cats, characterized by symptoms such as sneezing, itching, and difficulty breathing.
"Sutphin" Surname 38.9%
23andMe Users 36.7%
Migraine
A severe headache characterized by intense pain, sensitivity to light and sound, and often accompanied by nausea and vomiting.
"Sutphin" Surname 21.1%
23andMe Users 16.4%
Cat Allergy
An allergic reaction to cats, characterized by symptoms such as sneezing, itching, and difficulty breathing.
"Sutphin" Surname 38.9%
23andMe Users 36.7%
Migraine
A severe headache characterized by intense pain, sensitivity to light and sound, and often accompanied by nausea and vomiting.
"Sutphin" Surname 21.1%
23andMe Users 16.4%
Cat Allergy
An allergic reaction to cats, characterized by symptoms such as sneezing, itching, and difficulty breathing.
"Sutphin" Surname 38.9%
23andMe Users 36.7%
Are health conditions linked to the last name Sutphin?
The short answer is that, if there is an association between surname and health, it's usually more about your ancestry than your name. Individuals with a given surname are no more genetically similar than the general population but often have similar ancestries. The populations of people associated with those shared ancestries often have sets of genetic variations, also known as alleles, in common. Some of those alleles are associated with a greater likelihood of developing certain diseases.
Disease variant frequency by ancestry
Disease allele frequencies in populations associated with the surname Sutphin are shown below. Important Note: not everyone with a disease allele will develop these health condition
Age-Related Macular Degeneration
Y402H variant
Age-related macular degeneration (AMD) is the most common cause of irreversible vision loss among older adults. The disease results in damage to the central part of the retina (the macula), impairing vision needed for reading, driving, or even recognizing faces. The 23andMe Health + Ancestry DNA test includes the two most common variants associated with an increased risk of developing the condition: the Y402H variant in the CFH gene and the A69S variant in the ARMS2 gene. Learn more about Age-Related Macular Degeneration
British & Irish 62.1%
23andMe Users 57.2%
Hereditary Hemochromatosis (HFE-Related)
H63D variant
Hereditary hemochromatosis is a genetic condition characterized by absorption of too much dietary iron. This may lead to iron overload, which can cause damage to the joints and certain organs, such as the liver, skin, heart, and pancreas. The 23andMe Health + Ancestry DNA test includes the two most common variants linked to this condition. Learn more about Hereditary Hemochromatosis (HFE-Related)
British & Irish 28.3%
23andMe Users 25.0%
Late-Onset Alzheimer's Disease
ε4 variant
Alzheimer's disease is characterized by memory loss, cognitive decline, and personality changes. Late-onset Alzheimer's disease is the most common form of Alzheimer's disease, developing after age 65. Many factors, including genetics, can influence a person's chances of developing the condition. The 23andMe Health + Ancestry DNA test includes the most common genetic variant associated with late-onset Alzheimer's disease: the ε4 variant in the APOE gene. Learn more about Late-Onset Alzheimer's Disease
British & Irish 28.2%
23andMe Users 25.5%
Celiac Disease
HLA-DQ2.5 variant
Celiac disease is an autoimmune condition in which the consumption of gluten (found in wheat, barley, and rye) can result in damage to the small intestine. Celiac disease can lead to both digestive and non-digestive problems. The 23andMe Health + Ancestry DNA test includes two common variants associated with an increased risk of developing this condition. Learn more about Celiac Disease
British & Irish 27.7%
23andMe Users 21.4%
Celiac Disease
HLA-DQ8 variant
Celiac disease is an autoimmune condition in which the consumption of gluten (found in wheat, barley, and rye) can result in damage to the small intestine. Celiac disease can lead to both digestive and non-digestive problems. The 23andMe Health + Ancestry DNA test includes two common variants associated with an increased risk of developing this condition. Learn more about Celiac Disease
British & Irish 18.9%
23andMe Users 20.0%
Hereditary Hemochromatosis (HFE-Related)
C282Y variant
Hereditary hemochromatosis is a genetic condition characterized by absorption of too much dietary iron. This may lead to iron overload, which can cause damage to the joints and certain organs, such as the liver, skin, heart, and pancreas. The 23andMe Health + Ancestry DNA test includes the two most common variants linked to this condition. Learn more about Hereditary Hemochromatosis (HFE-Related)
British & Irish 17.6%
23andMe Users 9.8%
Alpha-1 Antitrypsin Deficiency
PI*S variant
AAT deficiency is a genetic condition that can lead to lung and liver disease. It is caused by decreased levels of the alpha-1 antitrypsin (AAT) protein. The 23andMe Health + Ancestry DNA test includes the two most common variants linked to this deficiency: the PI*S and PI*Z variants in the SERPINA1 gene. Learn more about Alpha-1 Antitrypsin Deficiency
British & Irish 9.5%
23andMe Users 7.3%
Hereditary Thrombophilia
Factor V Leiden variant
Hereditary thrombophilia is a predisposition to developing harmful blood clots. These harmful blood clots most commonly form in the legs and can travel to the lungs. The 23andMe Health + Ancestry DNA test includes the two most common variants linked to hereditary thrombophilia. Learn more about Hereditary Thrombophilia
British & Irish 4.2%
23andMe Users 4.5%
Alpha-1 Antitrypsin Deficiency
PI*Z variant
AAT deficiency is a genetic condition that can lead to lung and liver disease. It is caused by decreased levels of the alpha-1 antitrypsin (AAT) protein. The 23andMe Health + Ancestry DNA test includes the two most common variants linked to this deficiency: the PI*S and PI*Z variants in the SERPINA1 gene. Learn more about Alpha-1 Antitrypsin Deficiency
British & Irish 4.0%
23andMe Users 2.9%
Cystic Fibrosis
DeltaF508 variant
Cystic fibrosis is a rare genetic disorder characterized by impaired lung and digestive function. A person must have two variants in the CFTR gene in order to have this condition. Learn more about Cystic Fibrosis
British & Irish 3.5%
23andMe Users 2.3%
Age-Related Macular Degeneration
Y402H variant
Age-related macular degeneration (AMD) is the most common cause of irreversible vision loss among older adults. The disease results in damage to the central part of the retina (the macula), impairing vision needed for reading, driving, or even recognizing faces. The 23andMe Health + Ancestry DNA test includes the two most common variants associated with an increased risk of developing the condition: the Y402H variant in the CFH gene and the A69S variant in the ARMS2 gene. Learn more about Age-Related Macular Degeneration
British & Irish 62.1%
23andMe Users 57.2%
Hereditary Hemochromatosis (HFE-Related)
H63D variant
Hereditary hemochromatosis is a genetic condition characterized by absorption of too much dietary iron. This may lead to iron overload, which can cause damage to the joints and certain organs, such as the liver, skin, heart, and pancreas. The 23andMe Health + Ancestry DNA test includes the two most common variants linked to this condition. Learn more about Hereditary Hemochromatosis (HFE-Related)
British & Irish 28.3%
23andMe Users 25.0%
Late-Onset Alzheimer's Disease
ε4 variant
Alzheimer's disease is characterized by memory loss, cognitive decline, and personality changes. Late-onset Alzheimer's disease is the most common form of Alzheimer's disease, developing after age 65. Many factors, including genetics, can influence a person's chances of developing the condition. The 23andMe Health + Ancestry DNA test includes the most common genetic variant associated with late-onset Alzheimer's disease: the ε4 variant in the APOE gene. Learn more about Late-Onset Alzheimer's Disease
British & Irish 28.2%
23andMe Users 25.5%
Celiac Disease
HLA-DQ2.5 variant
Celiac disease is an autoimmune condition in which the consumption of gluten (found in wheat, barley, and rye) can result in damage to the small intestine. Celiac disease can lead to both digestive and non-digestive problems. The 23andMe Health + Ancestry DNA test includes two common variants associated with an increased risk of developing this condition. Learn more about Celiac Disease
British & Irish 27.7%
23andMe Users 21.4%
Celiac Disease
HLA-DQ8 variant
Celiac disease is an autoimmune condition in which the consumption of gluten (found in wheat, barley, and rye) can result in damage to the small intestine. Celiac disease can lead to both digestive and non-digestive problems. The 23andMe Health + Ancestry DNA test includes two common variants associated with an increased risk of developing this condition. Learn more about Celiac Disease
British & Irish 18.9%
23andMe Users 20.0%
Hereditary Hemochromatosis (HFE-Related)
C282Y variant
Hereditary hemochromatosis is a genetic condition characterized by absorption of too much dietary iron. This may lead to iron overload, which can cause damage to the joints and certain organs, such as the liver, skin, heart, and pancreas. The 23andMe Health + Ancestry DNA test includes the two most common variants linked to this condition. Learn more about Hereditary Hemochromatosis (HFE-Related)
British & Irish 17.6%
23andMe Users 9.8%
Alpha-1 Antitrypsin Deficiency
PI*S variant
AAT deficiency is a genetic condition that can lead to lung and liver disease. It is caused by decreased levels of the alpha-1 antitrypsin (AAT) protein. The 23andMe Health + Ancestry DNA test includes the two most common variants linked to this deficiency: the PI*S and PI*Z variants in the SERPINA1 gene. Learn more about Alpha-1 Antitrypsin Deficiency
British & Irish 9.5%
23andMe Users 7.3%
Hereditary Thrombophilia
Factor V Leiden variant
Hereditary thrombophilia is a predisposition to developing harmful blood clots. These harmful blood clots most commonly form in the legs and can travel to the lungs. The 23andMe Health + Ancestry DNA test includes the two most common variants linked to hereditary thrombophilia. Learn more about Hereditary Thrombophilia
British & Irish 4.2%
23andMe Users 4.5%
Alpha-1 Antitrypsin Deficiency
PI*Z variant
AAT deficiency is a genetic condition that can lead to lung and liver disease. It is caused by decreased levels of the alpha-1 antitrypsin (AAT) protein. The 23andMe Health + Ancestry DNA test includes the two most common variants linked to this deficiency: the PI*S and PI*Z variants in the SERPINA1 gene. Learn more about Alpha-1 Antitrypsin Deficiency
British & Irish 4.0%
23andMe Users 2.9%
Cystic Fibrosis
DeltaF508 variant
Cystic fibrosis is a rare genetic disorder characterized by impaired lung and digestive function. A person must have two variants in the CFTR gene in order to have this condition. Learn more about Cystic Fibrosis
British & Irish 3.5%
23andMe Users 2.3%
Age-Related Macular Degeneration
Y402H variant
Age-related macular degeneration (AMD) is the most common cause of irreversible vision loss among older adults. The disease results in damage to the central part of the retina (the macula), impairing vision needed for reading, driving, or even recognizing faces. The 23andMe Health + Ancestry DNA test includes the two most common variants associated with an increased risk of developing the condition: the Y402H variant in the CFH gene and the A69S variant in the ARMS2 gene. Learn more about Age-Related Macular Degeneration
British & Irish 62.1%
23andMe Users 57.2%
Hereditary Hemochromatosis (HFE-Related)
H63D variant
Hereditary hemochromatosis is a genetic condition characterized by absorption of too much dietary iron. This may lead to iron overload, which can cause damage to the joints and certain organs, such as the liver, skin, heart, and pancreas. The 23andMe Health + Ancestry DNA test includes the two most common variants linked to this condition. Learn more about Hereditary Hemochromatosis (HFE-Related)
British & Irish 28.3%
23andMe Users 25.0%
Late-Onset Alzheimer's Disease
ε4 variant
Alzheimer's disease is characterized by memory loss, cognitive decline, and personality changes. Late-onset Alzheimer's disease is the most common form of Alzheimer's disease, developing after age 65. Many factors, including genetics, can influence a person's chances of developing the condition. The 23andMe Health + Ancestry DNA test includes the most common genetic variant associated with late-onset Alzheimer's disease: the ε4 variant in the APOE gene. Learn more about Late-Onset Alzheimer's Disease
British & Irish 28.2%
23andMe Users 25.5%
Celiac Disease
HLA-DQ2.5 variant
Celiac disease is an autoimmune condition in which the consumption of gluten (found in wheat, barley, and rye) can result in damage to the small intestine. Celiac disease can lead to both digestive and non-digestive problems. The 23andMe Health + Ancestry DNA test includes two common variants associated with an increased risk of developing this condition. Learn more about Celiac Disease
British & Irish 27.7%
23andMe Users 21.4%
Celiac Disease
HLA-DQ8 variant
Celiac disease is an autoimmune condition in which the consumption of gluten (found in wheat, barley, and rye) can result in damage to the small intestine. Celiac disease can lead to both digestive and non-digestive problems. The 23andMe Health + Ancestry DNA test includes two common variants associated with an increased risk of developing this condition. Learn more about Celiac Disease
British & Irish 18.9%
23andMe Users 20.0%
Hereditary Hemochromatosis (HFE-Related)
C282Y variant
Hereditary hemochromatosis is a genetic condition characterized by absorption of too much dietary iron. This may lead to iron overload, which can cause damage to the joints and certain organs, such as the liver, skin, heart, and pancreas. The 23andMe Health + Ancestry DNA test includes the two most common variants linked to this condition. Learn more about Hereditary Hemochromatosis (HFE-Related)
British & Irish 17.6%
23andMe Users 9.8%
Alpha-1 Antitrypsin Deficiency
PI*S variant
AAT deficiency is a genetic condition that can lead to lung and liver disease. It is caused by decreased levels of the alpha-1 antitrypsin (AAT) protein. The 23andMe Health + Ancestry DNA test includes the two most common variants linked to this deficiency: the PI*S and PI*Z variants in the SERPINA1 gene. Learn more about Alpha-1 Antitrypsin Deficiency
British & Irish 9.5%
23andMe Users 7.3%
Hereditary Thrombophilia
Factor V Leiden variant
Hereditary thrombophilia is a predisposition to developing harmful blood clots. These harmful blood clots most commonly form in the legs and can travel to the lungs. The 23andMe Health + Ancestry DNA test includes the two most common variants linked to hereditary thrombophilia. Learn more about Hereditary Thrombophilia
British & Irish 4.2%
23andMe Users 4.5%
Alpha-1 Antitrypsin Deficiency
PI*Z variant
AAT deficiency is a genetic condition that can lead to lung and liver disease. It is caused by decreased levels of the alpha-1 antitrypsin (AAT) protein. The 23andMe Health + Ancestry DNA test includes the two most common variants linked to this deficiency: the PI*S and PI*Z variants in the SERPINA1 gene. Learn more about Alpha-1 Antitrypsin Deficiency
British & Irish 4.0%
23andMe Users 2.9%
Cystic Fibrosis
DeltaF508 variant
Cystic fibrosis is a rare genetic disorder characterized by impaired lung and digestive function. A person must have two variants in the CFTR gene in order to have this condition. Learn more about Cystic Fibrosis
British & Irish 3.5%
23andMe Users 2.3%