1 372414222218Reads by AI crawlersClaude2ChatGPT4Google · Gemini0Perplexity1Meta AI4Microsoft · Copilot2Amazon2Apple2China (ByteDance, Huawei, Baidu…)2ByteDance (Doubao)2Others18Total37Counted 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 382,500 European ancestry individuals.
The effect
Each copy of the C allele shifted the measure 0.0125 higher (95% confidence interval 0.0087-0.0164); p = 2 × 10−10.
How common The C allele had a frequency of about 23% in the people studied.
Where it sits Chromosome 5, band 5q12.3 — in an intron of CWC27.
What each result means
C/CTwo copies of the version the research linked to Urinary albumin excretion. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/GOne copy of the version the research linked to Urinary albumin excretion. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Urinary albumin excretion. This is the starting point the study compared everyone against.
American journal of human genetics · 2018 · PMID 30220432
Questions about rs7731168
What is rs7731168?
rs7731168 is a single position in the genome, in or near the CWC27 gene. Published research associates it with urinary albumin excretion. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs7731168 linked to?
On MyGeneLog this position is linked to Kidney Function. The research behind each link, and its sources, are set out on that condition page.
Does having rs7731168 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 rs7731168 come from?
GWAS Catalog, Am J Hum Genet 2018, PMID:30220432. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
1 372414222218Reads by AI crawlersClaude2ChatGPT4Google · Gemini0Perplexity1Meta AI4Microsoft · Copilot2Amazon2Apple2China (ByteDance, Huawei, Baidu…)2ByteDance (Doubao)2Others18Total37Counted 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
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Urinary albumin excretion (rs7731168). MyGeneLog™. https://www.mygenelog.com/variants/rs7731168