Sensitive

Skin cancer

RGS22 · rs113394050

Where this position leads

Condition: Sun Sensitivity, Freckling and Skin Cancer Risk

rs113394050 Condition: Sun Sensitivity, Freckling and Skin Cancer Risk Sun Sensitivity, Freckling and Skin… Condition rs113394050 rs113394050 RGS22

What the study found

Who was studied 25,928 European ancestry cases, 466,275 European ancestry controls, 154 East Asian ancestry cases, 178,572 East Asian ancestry controls.

The effect Each copy of the C allele shifted the measure 0.133 lower (95% confidence interval 0.11-0.16); p = 2 × 10−20.

Where it sits Chromosome 8, band 8q22.2 — in an intron of RGS22.

What each result means

C/C Two copies of the version the research linked to Skin 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 Skin cancer. That is a smaller link than two copies.
T/T No copy of the version the research linked to Skin cancer. This is the starting point the study compared everyone against.
Source

Questions about rs113394050

What is rs113394050?

rs113394050 is a single position in the genome, in or near the RGS22 gene. Published research associates it with skin 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 rs113394050 linked to?

On MyGeneLog this position is linked to Sun Sensitivity, Freckling and Skin Cancer Risk. The research behind each link, and its sources, are set out on that condition page.

Does having rs113394050 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 rs113394050 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

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Skin cancer (rs113394050). MyGeneLog™. https://www.mygenelog.com/variants/rs113394050

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