Breast cancer subtype (triple negative vs luminal A-like)
NR2F6 · rs77825513
0 8125Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity1Meta AI0Microsoft · Copilot0Amazon2Apple0China (ByteDance, Huawei, Baidu…)0Others5Total8Counted 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 16,499 European ancestry triple negative cases, 60,715 European ancestry luminal A-like cases.
The effect
Each copy of the A allele shifted the measure 0.022 higher (95% confidence interval 0.014-0.03); p = 1 × 10−9.
Where it sits Chromosome 19, band 19p13.11 — in an intron of NR2F6.
What each result means
A/ATwo copies of the version the research linked to Breast cancer subtype (triple negative vs luminal A-like). That is the strongest link of the three results. A link in a study is not a diagnosis.
A/COne copy of the version the research linked to Breast cancer subtype (triple negative vs luminal A-like). That is a smaller link than two copies.
C/CNo copy of the version the research linked to Breast cancer subtype (triple negative vs luminal A-like). This is the starting point the study compared everyone against.
rs77825513 is a single position in the genome, in or near the NR2F6 gene. Published research associates it with breast cancer subtype (triple negative vs luminal a-like). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs77825513 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 rs77825513 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 rs77825513 come from?
GWAS Catalog, Cancer research 2024, PMID:38832928. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
0 8125Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity1Meta AI0Microsoft · Copilot0Amazon2Apple0China (ByteDance, Huawei, Baidu…)0Others5Total8Counted 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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Breast cancer subtype (triple negative vs luminal A-like) (rs77825513). MyGeneLog™. https://www.mygenelog.com/variants/rs77825513