5 433216123223Reads by AI crawlersClaude3ChatGPT2Google · Gemini0Perplexity1Meta AI6Microsoft · Copilot1Amazon2Apple3China (ByteDance, Huawei, Baidu…)2ByteDance (Doubao)2Others23Total43Counted 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 11,816 Han Chinese ancestry individuals; replicated in 69,146 Han Chinese ancestry individuals.
The effect
Each copy of the T allele shifted the measure 1.24 higher (95% confidence interval 0.95-1.53); p = 6 × 10−17.
How common The T allele had a frequency of about 71% in the people studied.
Where it sits Chromosome 10, band 10q24.32 — in an intron of BORCS7.
What each result means
C/CNo copy of the version the research linked to Systolic blood pressure. This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Systolic blood pressure. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Systolic blood pressure. That is the strongest link of the three results. A link in a study is not a diagnosis.
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 rs4409766
What is rs4409766?
rs4409766 is a single position in the genome, in or near the CYP17A1 gene. Published research associates it with systolic blood pressure. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs4409766 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 rs4409766?
Subjects that appear in the title or abstract of the same papers as this rsID include 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 rs4409766 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 rs4409766 come from?
GWAS Catalog, Hum Mol Genet 2014, PMID:25249183. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
5 433216123223Reads by AI crawlersClaude3ChatGPT2Google · Gemini0Perplexity1Meta AI6Microsoft · Copilot1Amazon2Apple3China (ByteDance, Huawei, Baidu…)2ByteDance (Doubao)2Others23Total43Counted 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.
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