A/APublished research associates this genotype with typical/baseline likelihood of Body mass index — no copies of the reported risk allele.
A/CPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with Body mass index.
C/CPublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Body mass index compared to the general population.
Nature genetics · 2013 · PMID 23583978 · open access
Questions about rs10261878
What is rs10261878?
rs10261878 is a single position in the genome, in or near the NFE2L3 gene. Published research associates it with body mass index. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs10261878 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.
Does having rs10261878 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 rs10261878 come from?
GWAS Catalog, Nat Genet 2013, PMID:23583978. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.