Standard

Obesity

GNPDA2 · rs10938397

Where this position leads

Condition: Obesity and Body Weight

rs10938397 Condition: Obesity and Body Weight Obesity and Body Weight Condition rs10938397 rs10938397 GNPDA2

What each result means

A/A Published research associates this genotype with typical/baseline likelihood of Obesity — no copies of the reported risk allele. (GWAS Catalog, Nat Genet 2013, PMID:23563607)
A/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Obesity. (GWAS Catalog, Nat Genet 2013, PMID:23563607)
G/G Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Obesity compared to the general population. (GWAS Catalog, Nat Genet 2013, PMID:23563607)

Source: GWAS Catalog, Nat Genet 2013, PMID:23563607

What people read about alongside this

Papers in Europe PMC whose title or abstract names both this rsID and that subject. A shared paper means somebody wrote about the two together — it is not a claim that this position explains the subject.

Questions about rs10938397

What is rs10938397?

rs10938397 is a single position in the genome, in or near the GNPDA2 gene. Published research associates it with obesity. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs10938397 linked to?

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

What do people read about alongside rs10938397?

Subjects that appear in the title or abstract of the same papers as this rsID include exercise and muscle (2 papers), adhd and attention (1 papers), risk-taking and impulsivity (1 papers). A shared paper means somebody wrote about the two together; it is not a claim that this position explains the topic.

Does having rs10938397 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 rs10938397 come from?

GWAS Catalog, Nat Genet 2013, PMID:23563607. 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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