Sensitive

Prostate cancer

LINC00506 · rs9310048

Where this position leads

Condition: Prostate Cancer

rs9310048 Condition: Prostate Cancer Prostate Cancer Condition rs9310048 rs9310048 LINC00506

What the study found

Who was studied 5,672 East Asian ancestry cases, 84,660 East Asian ancestry controls.

The effect Each copy of the C allele shifted the measure 0.198 higher (95% confidence interval 0.15-0.25); p = 2 × 10−15.

How common The C allele had a frequency of about 22% in the people studied.

Where it sits Chromosome 3, band 3p11.2 — in an intron of LINC00506.

What each result means

C/C Two copies of the version the research linked to Prostate cancer. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/T One copy of the version the research linked to Prostate cancer. That is a smaller link than two copies.
T/T No copy of the version the research linked to Prostate cancer. This is the starting point the study compared everyone against.
Source

Questions about rs9310048

What is rs9310048?

rs9310048 is a single position in the genome, in or near the LINC00506 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 rs9310048 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 rs9310048 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 rs9310048 come from?

GWAS Catalog, Nature genetics 2021, PMID:34594039. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

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.

Prostate cancer (rs9310048). MyGeneLog™. https://www.mygenelog.com/variants/rs9310048

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