rs237902
This is a synonymous variant in the OXTR gene — it does not change the protein's amino acid sequence.
▶ClinVar annotation
▶Research that mentions this SNP (2)
▶NOS‐I and ‐III gene variants are differentially associated with facets of suicidal behavior and aggression‐related traitsReviewDan Rujescu et al.(2008)· American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
A comprehensive review of the genetic basis of aggressive behavior, covering candidate genes in neurotransmitter systems (TPH1, TPH2, SLC6A4, DRD4, COMT, MAOA), hypothalamic-pituitary genes (OXT, OXTR, AVPR1A, AVPR1B), and GWAS findings (LRRTM4 rs11126630 p=5.30×10⁻⁸, CDH13 rs11649622 p=4.19×10⁻⁶, FYN rs2148710 p=2.9×10⁻⁸, DYRK1A). The review concludes that genetic predisposition to aggressive behavior involves multiple genes with small individual effects (1-2% each).
▶A Polymorphism in the Serotonin Receptor 3A (HTR3A) Gene and Its Association With Harm Avoidance in WomenAssociationN=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.
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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