0 22281236Reads by AI crawlersClaude0ChatGPT2Google · Gemini0Perplexity0Meta AI8Microsoft · Copilot1Amazon2Apple3China (ByteDance, Huawei, Baidu…)0Others6Total22Counted 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 17,416 European ancestry cases, 375,455 European ancestry controls.
The effect
Each copy of the T allele shifted the measure 0.199 lower (95% confidence interval 0.16-0.24); p = 2 × 10−25.
How common The T allele had a frequency of about 10% in the people studied.
Where it sits Chromosome 2, band 2p24.3 — between genes, 45.4 kb from LOC107985855.
What each result means
G/GNo copy of the version the research linked to Basal cell carcinoma. This is the starting point the study compared everyone against.
G/TOne copy of the version the research linked to Basal cell carcinoma. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Basal cell carcinoma. That is the strongest link of the three results. A link in a study is not a diagnosis.
Genome medicine · 2021 · PMID 33549134 · open access
Questions about rs340797
What is rs340797?
rs340797 is a single position in the genome, in or near the FAM49A gene. Published research associates it with basal cell carcinoma. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs340797 linked to?
On MyGeneLog this position is linked to Basal Cell Carcinoma. The research behind each link, and its sources, are set out on that condition page.
Does having rs340797 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 rs340797 come from?
GWAS Catalog, Genome Med 2021, PMID:33549134. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
0 22281236Reads by AI crawlersClaude0ChatGPT2Google · Gemini0Perplexity0Meta AI8Microsoft · Copilot1Amazon2Apple3China (ByteDance, Huawei, Baidu…)0Others6Total22Counted 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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