Standard
Morning vs. evening chronotype
FAT1 · rs148750727
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
G/G
Published research associates this genotype with typical/baseline likelihood of Morning vs. evening chronotype — no copies of the reported risk allele.
G/T
Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Morning vs. evening chronotype.
T/T
Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Morning vs. evening chronotype compared to the general population.
Source
Genome-wide association analysis identifies novel loci for chronotype in 100,420 individuals from the UK Biobank
Lane JM,
Vlasac I,
Anderson SG,
Kyle SD,
Dixon WG,
Bechtold DA,
Gill S,
Little MA,
Luik A,
Loudon A,
Emsley R,
Scheer FA
and 6 more — show all
Nature communications · 2016 · PMID 26955885 · open access
Questions about rs148750727
What is rs148750727?
rs148750727 is a single position in the genome, in or near the FAT1 gene. Published research associates it with morning vs. evening chronotype. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs148750727 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 rs148750727 come from?
GWAS Catalog, Nat Commun 2016, PMID:26955885. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
← See all variants