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Who was studied 3,238 East Asian ancestry cases, 4,083 East Asian ancestry controls.
The effect
Each copy of the C allele carried 11.00 times the odds of Epithelial ovarian cancer (95% confidence interval 5.3-24); p = 3 × 10−10.
How common The C allele had a frequency of about 94% in the people studied.
Where it sits Chromosome 10, band 10p12.1 — in an intron of LINC02652.
What each result means
C/CTwo copies of the version the research linked to Epithelial ovarian cancer. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/GOne copy of the version the research linked to Epithelial ovarian cancer. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Epithelial ovarian cancer. This is the starting point the study compared everyone against.
rs1934363 is a single position in the genome, in or near the LINC02652 gene. Published research associates it with epithelial ovarian 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 rs1934363 linked to?
On MyGeneLog this position is linked to Ovarian Cancer. The research behind each link, and its sources, are set out on that condition page.
Does having rs1934363 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 rs1934363 come from?
GWAS Catalog, Gynecologic oncology 2019, PMID:30898391. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
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Quoting this page
Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.
Epithelial ovarian cancer (rs1934363). MyGeneLog™. https://www.mygenelog.com/variants/rs1934363