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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
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
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)
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
The ethnic identity of those bearing the surname Harvey also saw changes between 2000 and 2010, as per the Decennial U.S. Census. Although the majority of individuals who identify as Harvey are White (68.00%), there was a slight decrease in this group by -3.82% between 2000 and 2010. The largest increase occurred within the Hispanic community, rising by 59.49%, while the Asian/Pacific Islander and Two or more races communities also saw substantial increases of 26.83% and 36.36% respectively. The American Indian and Alaskan Native community saw a moderate increase of 9.62%, and the Black community saw a small increase of 3.69%.
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)
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 Harvey is British & Irish, which comprises 53.4% of all ancestry found in people with the surname. The next two most common ancestries are French & German (21.9%) and Eastern European (3.5%). Additional ancestries include Scandinavian, Nigerian, Italian, Spanish & Portuguese, and Ghanaian, Liberian & Sierra Leonean.
Based on 23andMe data, people with last name Harvey have recent ancestry locations all within the United Kingdom of Great Britain and Northern Ireland.
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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
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
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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.
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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.
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)
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
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
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)
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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
The top paternal haplogroup of people with the surname Harvey is R-CTS241, which is predominantly found among people with European ancestry. Haplogroup R-CTS241 is descended from haplogroup R-M343. Other common haplogroups include R-U152 and R-P311, which are predominantly found among people with European and European ancestry. Other surnames with similar common haplogroups are: Wilson, Smith, Thompson, Brown, Taylor, Clark, Young, White, Mitchell, Miller.
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
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.
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)
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
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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
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A severe headache characterized by intense pain, sensitivity to light and sound, and often accompanied by nausea and vomiting.
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
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
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
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
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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.
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
1. English (of Norman origin): from the Old French and Middle English personal name Hervei, also found as Herveu, Hervé, and Hervi. The name Herveu or Herv(e)i was borne by a number of Bretons at the Norman Conquest and, as such, represents a French form of the Old Breton name Hoiearnviu or Hærviu (see Herve). Among Normans Herve(i) or Herv(e)i was also a French form of ancient Germanic Hariwic, Herewic (from hari ‘army’ + wīg ‘war’), with intervocalic /w/ becoming /v/ in Old French. The Breton and ancient Germanic names were commonly Latinized as Herve(i)us and Hervic(i)us respectively but, since their most common vernacular forms in Old French were indistinguishable, the Latin forms were also sometimes interchangeable, especially Herveus. 2. Irish: shortened Anglicized form of Gaelic Ó hAirmheadhaigh ‘descendant of Airmheadhach’, a personal name probably meaning ‘esteemed’. It seems to be a derivative of Airmheadh, the name borne by a mythological physician. 3. Irish: shortened Anglicized form of Gaelic Ó hEarchaidh ‘descendant of Earchadh’, a personal name of uncertain origin. 4. Irish: sometimes identical with 1, especially through migration from southwest Scotland. 5. Altered form of Breton Hervé (see Herve), a cognate of 1 above.
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Disease allele frequencies in populations associated with the surname Harvey are shown below. Important Note: not everyone with a disease allele will develop these health condition
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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
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A severe headache characterized by intense pain, sensitivity to light and sound, and often accompanied by nausea and vomiting.
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)
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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
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
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
According to data from the Decennial U.S. Census, the popularity of the surname Harvey has seen a slight decrease in rank between 2000 and 2010, moving from the 247th most common surname to the 266th. Despite this drop in rank, the total count of individuals with the surname Harvey actually increased by 3.14% during the same time period. However, when adjusted for population growth, the proportion of individuals named Harvey per 100,000 people decreased by 5.68%.
A severe headache characterized by intense pain, sensitivity to light and sound, and often accompanied by nausea and vomiting.
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
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
The most common maternal haplogroups of people with Harvey surname are: H1, T2b, H. These most commonly trace back to individuals of European ancestry.
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.
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
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