rs10012282 - WDR17

Magnitude 4.5 · 1 study on file

Reported associations

• Genome-wide Analysis of Insomnia Disorder - Unknown journal (n.d.) · Unknown authors · PubMed 29520036

  ABSTRACT: Insomnia is a worldwide problem with substantial deleterious health effects. Twin studies have shown a heritable basis for various sleep-related traits, including insomnia, but robust genetic risk variants have just recently begun to be identified. We conducted genome-wide association studies (GWAS) of soldiers in the Army Study To Assess Risk and Resilience in Servicemembers (STARRS). GWAS were carried out separately for each ancestral group (EUR, AFR, LAT) using logistic regression for each of the STARRS component studies (including 3,237 cases and 14,414 controls), and then meta-analysis was conducted across studies and ancestral groups. Heritability (SNP-based) for lifetime insomnia disorder was significant (h2g=0.115, p=1.78×10−4 in EUR). A meta-analysis including three a

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