rs2042126

This variant is located in the NAALADL2 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 NAALADL2

Predicted to act upstream of or within response to bacterium. Located in nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]

View all NAALADL2 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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