0 181112310Reads by AI crawlersClaude0ChatGPT0Google · Gemini1Perplexity1Meta AI0Microsoft · Copilot1Amazon2Apple3China (ByteDance, Huawei, Baidu…)0Others10Total18Counted 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 295,529 European ancestry individuals, 8,231 Latino individuals, 3,058 African American individuals, 2,029 African British individuals, 7,701 East Asian ancestry individuals, 2,735 South Asian ancestry individuals, 1,979 mixed and unknown ancestry individuals.
The effect
Each copy of the G allele shifted the measure 0.584 lower; p = 1 × 10−22.
Where it sits Chromosome 17, band 17q21.32 — between genes, 3.4 kb from WNT9B.
What each result means
A/ANo copy of the version the research linked to Systolic blood pressure. This is the starting point the study compared everyone against.
A/GOne copy of the version the research linked to Systolic blood pressure. That is a smaller link than two copies.
G/GTwo 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.
Nature genetics · 2017 · PMID 27841878 · open access
Questions about rs75230966
What is rs75230966?
rs75230966 is a single position in the genome, in or near the near WNT9B 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 rs75230966 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.
Does having rs75230966 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 rs75230966 come from?
GWAS Catalog, Nat Genet 2016, PMID:27841878. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
0 181112310Reads by AI crawlersClaude0ChatGPT0Google · Gemini1Perplexity1Meta AI0Microsoft · Copilot1Amazon2Apple3China (ByteDance, Huawei, Baidu…)0Others10Total18Counted 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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