18 60141536222124Reads by AI crawlersClaude1ChatGPT4Google · Gemini15Perplexity3Meta AI6Microsoft · Copilot2Amazon2Apple2China (ByteDance, Huawei, Baidu…)1ByteDance (Doubao)1Others24Total60Counted by the name each crawler declares; requests found to be impersonating one are left out. Google · Gemini includes Googlebot, the search crawler whose index Google also uses for its AI features. Other search engines and bots are under Others.
Solid lines are connections this site curates. Dashed lines mean the two ends share a research paper — worth knowing, and not a claim that one explains the other.
What each result means
Del/DelNeither copy carries the O-associated deletion — associated with blood type A, B, or AB, depending on other ABO gene variants not covered by this single marker.
Ins/DelOne copy of the O-associated deletion marker and one copy of the intact sequence — associated with blood type A or B, depending on other ABO gene variants not covered by this single marker.
Ins/InsThis variant is a deletion marker for the ABO gene's O allele. Two copies (Ins/Ins, meaning the functional-enzyme-disrupting insertion is present on both copies) is associated with blood type O.
This single marker narrows down but does not fully determine ABO blood type on its own — a clinical blood type test is the reliable way to know your type for medical purposes (e.g. transfusion, pregnancy).
Papers in Europe PMC whose title or abstract names both this rsID and that subject. A shared paper means somebody wrote about the two together — it is not a claim that this position explains the subject.
Questions about rs8176719
What is rs8176719?
rs8176719 is a single position in the genome, in or near the ABO gene. Published research associates it with abo blood type. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs8176719 linked to?
On MyGeneLog this position is linked to ABO Blood Group, Venous Thromboembolism. The research behind each link, and its sources, are set out on that condition page.
What do people read about alongside rs8176719?
Subjects that appear in the title or abstract of the same papers as this rsID include heart and circulation (4 papers), longevity and ageing (2 papers), cholesterol and blood fats (1 papers), personality (1 papers). A shared paper means somebody wrote about the two together; it is not a claim that this position explains the topic.
Does having rs8176719 mean I will get this?
No. Common variants like this one move a probability slightly and, on their own, rarely decide anything about one person. Nothing on this page is a diagnosis, and health decisions should be made with a clinician who can see your whole picture.
Where does the information about rs8176719 come from?
Yamamoto et al. 1990, Nature — molecular genetic basis of the histo-blood group ABO system. PMID 2333095. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
18 60141536222124Reads by AI crawlersClaude1ChatGPT4Google · Gemini15Perplexity3Meta AI6Microsoft · Copilot2Amazon2Apple2China (ByteDance, Huawei, Baidu…)1ByteDance (Doubao)1Others24Total60Counted by the name each crawler declares; requests found to be impersonating one are left out. Google · Gemini includes Googlebot, the search crawler whose index Google also uses for its AI features. Other search engines and bots are under Others.
Quoting this page
Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.
ABO blood type (rs8176719). MyGeneLog™. https://www.mygenelog.com/variants/rs8176719