Sensitive

Basal cell carcinoma

RGS22 · rs28765982

Where this position leads

Condition: Basal Cell Carcinoma

rs28765982 Condition: Basal Cell Carcinoma Basal Cell Carcinoma Condition rs28765982 rs28765982 RGS22

What the study found

Who was studied 49,905 European ancestry cases, 752,392 European ancestry controls, 626 Hispanic or Latin American cases, 9,842 Hispanic or Latin American controls.

The effect The reported allele is C; the catalogue records no effect size ; p = 3 × 10−63.

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

What each result means

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

Questions about rs28765982

What is rs28765982?

rs28765982 is a single position in the genome, in or near the RGS22 gene. Published research associates it with basal cell carcinoma. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs28765982 linked to?

On MyGeneLog this position is linked to Basal Cell Carcinoma. The research behind each link, and its sources, are set out on that condition page.

Does having rs28765982 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 rs28765982 come from?

GWAS Catalog, Communications biology 2024, PMID:38182794. 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.

Basal cell carcinoma (rs28765982). MyGeneLog™. https://www.mygenelog.com/variants/rs28765982

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