rs61740241

This variant is located in the OXTR gene.

ClinVar annotation

Benign
1 submitter

OXTR-related disorder

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Research that mentions this SNP (1)

A Polymorphism in the Serotonin Receptor 3A (HTR3A) Gene and Its Association With Harm Avoidance in Women
AssociationN=99Jonas Melke et al.(2003)· Archives of General Psychiatry

A candidate gene association study of 99 healthy Caucasian subjects examining OXTR (oxytocin receptor) variants rs237900 and rs237902 and their effects on personality traits. The study found sexually dimorphic effects on Harm Avoidance, with female carriers of the minor (T) alleles scoring significantly higher (rs237900: p=0.006, rs237902: p=0.01). When sex was controlled for and a sex*genotype interaction term was included in the regression model, the variants explained 11% of the variance in Harm Avoidance (p≤0.01). A novel A217T missense mutation was identified in a highly harm-avoidant male participant.

Traits studied:Harm AvoidancePersonality traits

About OXTR

The protein encoded by this gene belongs to the G-protein coupled receptor family and acts as a receptor for oxytocin. Its activity is mediated by G proteins which activate a phosphatidylinositol-calcium second messenger system. The oxytocin-oxytocin receptor system plays an important role in the uterus during parturition. [provided by RefSeq, Jul 2008]

View all OXTR variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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