rs17737465

This is a upstream gene variant variant in the CPQ gene.

Research that mentions this SNP (1)

A genome‐wide association study of sleep habits and insomnia
AssociationN=4,357Enda M. Byrne et al.(2013)· American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Genome-wide association study of 2,323 Australian twins identified several associations with sleep phenotypes including sleep latency, sleep quality, sleep duration, and insomnia, but no genome-wide significant variants. Most notable finding: SNPs in CACNA1C intron 3 (rs7316184, rs7304986, rs7301906, and others) showed strongest association with sleep latency (p = 1.3 × 10⁻⁶), though this did not replicate in independent Chronogen Consortium sample. Additional associations with insomnia factor score (rs11174478 in SLC2A13, p = 1.92 × 10⁻⁶) and sleep duration (rs4780805, p = 2.66 × 10⁻⁶) were identified but remain unreplicated.

Traits studied:InsomniaSleep depthSleep durationSleep latencySleep qualitySleeptime

About CPQ

This gene encodes a metallopeptidase that belongs to the peptidase M28 family. The encoded protein may catalyze the cleavage of dipeptides with unsubstituted terminals into amino acids. [provided by RefSeq, Jul 2013]

View all CPQ variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

Community Wiki

No community notes yet for this variant. Sign in to start one.

Comments

Sign in to join the discussion.

Loading comments…