Standard
Chronotype
FBXL13 · rs372229746
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
A/A
Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Chronotype compared to the general population.
A/G
Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Chronotype.
G/G
Published research associates this genotype with typical/baseline likelihood of Chronotype — no copies of the reported risk allele.
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 rs372229746
What is rs372229746?
rs372229746 is a single position in the genome, in or near the FBXL13 gene. Published research associates it with chronotype. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs372229746 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 rs372229746 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