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DNA methylation (parent-of-origin)

RPL26P31 · rs7931462

What each result means

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

Questions about rs7931462

What is rs7931462?

rs7931462 is a single position in the genome, in or near the RPL26P31 gene. Published research associates it with dna methylation (parent-of-origin). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs7931462 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 rs7931462 come from?

GWAS Catalog, Twin Res Hum Genet 2013, PMID:23725790. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

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