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Prostate-specific antigen levels

near RGS22 · rs115346150

What the study found

Who was studied 61,745 African ancestry individuals, 6,967 Asian ancestry individuals, 297,166 European ancestry individuals, 26,644 Hispanic or Latin American individuals.

The effect Each copy of the A allele shifted the measure 0.0349 higher (95% confidence interval 0.026-0.044); p = 4 × 10−15.

Where it sits Chromosome 8, band 8q22.2 — between genes, 6.1 kb from RGS22.

What each result means

A/A Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Prostate-specific antigen levels compared to the general population.
A/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Prostate-specific antigen levels.
G/G Published research associates this genotype with typical/baseline likelihood of Prostate-specific antigen levels — no copies of the reported risk allele.
Source

Questions about rs115346150

What is rs115346150?

rs115346150 is a single position in the genome, in or near the near RGS22 gene. Published research associates it with prostate-specific antigen levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs115346150 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 rs115346150 come from?

GWAS Catalog, Nature genetics 2025, PMID:39930085. 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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Prostate-specific antigen levels (rs115346150). MyGeneLog™. https://www.mygenelog.com/variants/rs115346150

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