Orviva

Learn · Variants · CLOCK

rs1801260 CLOCK

CLOCK gene variant associated with evening chronotype (night owl tendency).

Curated · human-reviewed Trait · Risk / effect allele: C · dbSNP

What is rs1801260?

rs1801260 is a single-nucleotide polymorphism (SNP) in the CLOCK gene (Circadian locomotor output cycles kaput). Each person carries two copies, one from each parent, so a result is reported as a pair of letters such as CC. The table below describes what studies associate with each genotype; the association is statistical, across populations, and is not a diagnosis.

What does each rs1801260 genotype mean?

GenotypeAssociationWhat the evidence saysConfidence
CCtypical / lowerCLOCK gene variant associated with evening chronotype (night owl tendency).70%
TC / CTtypical / lowerIntermediate chronotype.68%
TTtypical / lowerMorning chronotype tendency (early bird).70%

How common is the C allele of rs1801260?

Minor-allele frequency by population (gnomAD / 1000 Genomes):

European27.0%
East Asian15.0%
African20.0%
South Asian22.0%
Admixed American24.0%
Global22.0%

Which drugs have annotations for rs1801260?

PharmGKB clinical annotations (level 1A is the strongest evidence, 4 the weakest):

DrugAnnotation typeEvidence level
lithiumToxicity4

Is rs1801260 on 23andMe and AncestryDNA chips?

Yes — it is genotyped directly on 23andMe V3, 23andMe V4, 23andMe V5, AncestryDNA V1, AncestryDNA V2. Orviva reads it from a raw-data export without imputation.

Sources

Genetic associations describe risk across populations, not a diagnosis for any one person. Most variants shift risk modestly and act alongside lifestyle, environment and other genes. Consumer DNA chips do not read every position and can be wrong at any single one. For general education only; talk to a clinician or genetic counsellor before acting on anything here, and never change a prescribed medicine without your prescriber.