G/GPublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Prostate cancer compared to the general population.
G/TPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with Prostate cancer.
T/TPublished research associates this genotype with typical/baseline likelihood of Prostate cancer — no copies of the reported risk allele.
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2014 · PMID 24753544
Questions about rs12682344
What is rs12682344?
rs12682344 is a single position in the genome, in or near the SRRM1P1 gene. Published research associates it with prostate cancer. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs12682344 linked to?
On MyGeneLog this position is linked to Prostate Cancer. The research behind each link, and its sources, are set out on that condition page.
Does having rs12682344 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 rs12682344 come from?
GWAS Catalog, Cancer Epidemiol Biomarkers Prev 2014, PMID:24753544. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.