0 131210Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity1Meta AI0Microsoft · Copilot0Amazon2Apple0China (ByteDance, Huawei, Baidu…)0Others10Total13Counted 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 2,603 Korean ancestry males, 2,869 Korean ancestry females; replicated in 19,571 Korean ancestry males, 37,321 Korean ancestry females.
The effect
Each copy of the T allele shifted the measure 0.56 lower (95% confidence interval 0.46-0.66); p = 3 × 10−33.
How common The T allele had a frequency of about 17% in the people studied.
Where it sits Chromosome 12, band 12q13.2 — between genes, 3.4 kb from RNF41.
What each result means
C/CNo copy of the version the research linked to Height. This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Height. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Height. That is the strongest link of the three results. A link in a study is not a diagnosis.
Frontiers in genetics · 2021 · PMID 34054925 · open access
Questions about rs76459740
What is rs76459740?
rs76459740 is a single position in the genome, in or near the near RNF41 gene. Published research associates it with height. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs76459740 linked to?
On MyGeneLog this position is linked to Height. The research behind each link, and its sources, are set out on that condition page.
Does having rs76459740 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 rs76459740 come from?
GWAS Catalog, Frontiers in genetics 2021, PMID:34054925. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
0 131210Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity1Meta AI0Microsoft · Copilot0Amazon2Apple0China (ByteDance, Huawei, Baidu…)0Others10Total13Counted 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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