Standard
Daytime nap
FIGN · rs80163246
Stands on its own.
Nothing else here links to this position yet — but the page above is the point: what the
research found, what each genotype means, and where it came from, in language you can
read. Links to conditions, drugs and the senses appear automatically if we write them.
What each result means
C/C
Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Daytime nap compared to the general population. (GWAS Catalog, Nat Commun 2021, PMID:33568662)
C/T
Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Daytime nap. (GWAS Catalog, Nat Commun 2021, PMID:33568662)
T/T
Published research associates this genotype with typical/baseline likelihood of Daytime nap — no copies of the reported risk allele. (GWAS Catalog, Nat Commun 2021, PMID:33568662)
Source
Genetic determinants of daytime napping and effects on cardiometabolic health
Dashti HS,
Daghlas I,
Lane JM,
Huang Y,
Udler MS,
Wang H,
Ollila HM,
Jones SE,
Kim J,
Wood AR,
Weedon MN,
Aslibekyan S
and 2 more — show all
Nature communications · 2021 · PMID 33568662 · open access
Questions about rs80163246
What is rs80163246?
rs80163246 is a single position in the genome, in or near the FIGN gene. Published research associates it with daytime nap. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs80163246 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 rs80163246 come from?
GWAS Catalog, Nat Commun 2021, PMID:33568662. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
← See all variants