7 5422537222227Reads by AI crawlersClaude2ChatGPT2Google · Gemini5Perplexity3Meta AI7Microsoft · Copilot2Amazon2Apple2China (ByteDance, Huawei, Baidu…)2ByteDance (Doubao)2Others27Total54Counted 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.
Who was studied 29,136 European ancestry individuals; replicated in 34,433 European ancestry individuals.
The effect
Each copy of the A allele shifted the measure 0.15 log odds higher (95% confidence interval 0.11-0.19); p = 2 × 10−11.
How common The A allele had a frequency of about 83% in the people studied.
Where it sits Chromosome 12, band 12q21.33 — in an intron of ATP2B1.
What each result means
A/ATwo copies of the version the research linked to Hypertension. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/GOne copy of the version the research linked to Hypertension. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Hypertension. This is the starting point the study compared everyone against.
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 rs2681472
What is rs2681472?
rs2681472 is a single position in the genome, in or near the ATP2B1 gene. Published research associates it with hypertension. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs2681472 linked to?
On MyGeneLog this position is linked to Blood Pressure. The research behind each link, and its sources, are set out on that condition page.
What do people read about alongside rs2681472?
Subjects that appear in the title or abstract of the same papers as this rsID include blood sugar and insulin (2 papers), alcohol and the flush (1 papers), heart and circulation (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 rs2681472 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 rs2681472 come from?
GWAS Catalog, Nat Genet 2009, PMID:19430479. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
7 5422537222227Reads by AI crawlersClaude2ChatGPT2Google · Gemini5Perplexity3Meta AI7Microsoft · Copilot2Amazon2Apple2China (ByteDance, Huawei, Baidu…)2ByteDance (Doubao)2Others27Total54Counted 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.