Standard

Obesity

FTO · rs1558902

Where this position leads

Condition: Obesity and Body Weight

rs1558902 Condition: Obesity and Body Weight Obesity and Body Weight Condition rs1558902 rs1558902 FTO

What each result means

A/A 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)
A/T 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)
T/T 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)

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 rs1558902

What is rs1558902?

rs1558902 is a single position in the genome, in or near the FTO 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 rs1558902 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 rs1558902?

Subjects that appear in the title or abstract of the same papers as this rsID include brain and memory (2 papers), exercise and muscle (1 papers), smoking and vaping (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 rs1558902 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 rs1558902 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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