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CRIP2 protein levels

MTA1 · rs60837482

What the study found

Who was studied 47,745 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.171 lower (95% confidence interval 0.13-0.21); p = 4 × 10−15.

How common The T allele had a frequency of about 2% in the people studied.

Where it sits Chromosome 14, band 14q32.33 — in an intron of MTA1.

What each result means

C/C Published research associates this genotype with typical/baseline likelihood of CRIP2 protein levels — no copies of the reported risk allele.
C/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with CRIP2 protein levels.
T/T Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of CRIP2 protein levels compared to the general population.
Source

Questions about rs60837482

What is rs60837482?

rs60837482 is a single position in the genome, in or near the MTA1 gene. Published research associates it with crip2 protein levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs60837482 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 rs60837482 come from?

GWAS Catalog, Nature genetics 2025, PMID:39789286. 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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CRIP2 protein levels (rs60837482). MyGeneLog™. https://www.mygenelog.com/variants/rs60837482

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