0 110Reads by AI crawlersClaude1ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon0Apple0China (ByteDance, Huawei, Baidu…)0Others0Total1Counted 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 35,474 European ancestry UL cases, 133,384 European ancestry BC cases, 381,294 European ancestry controls.
The effect
The reported allele is T; the catalogue records no effect size
; p = 4 × 10−9.
Where it sits Chromosome 16, band 16q13 — in the 3′ untranslated region of GNAO1.
What each result means
C/CNo copy of the version the research linked to Uterine leiomyoma or breast cancer (pleiotropy). This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Uterine leiomyoma or breast cancer (pleiotropy). That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Uterine leiomyoma or breast cancer (pleiotropy). That is the strongest link of the three results. A link in a study is not a diagnosis.
American journal of human genetics · 2022 · PMID 35803233
Questions about rs3790110
What is rs3790110?
rs3790110 is a single position in the genome, in or near the GNAO1 gene. Published research associates it with uterine leiomyoma or breast cancer (pleiotropy). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs3790110 linked to?
On MyGeneLog this position is linked to Breast Cancer. The research behind each link, and its sources, are set out on that condition page.
Does having rs3790110 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 rs3790110 come from?
GWAS Catalog, American journal of human genetics 2022, PMID:35803233. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
0 110Reads by AI crawlersClaude1ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon0Apple0China (ByteDance, Huawei, Baidu…)0Others0Total1Counted 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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Uterine leiomyoma or breast cancer (pleiotropy) (rs3790110). MyGeneLog™. https://www.mygenelog.com/variants/rs3790110