rs53576, OXTR;CAV3

N. diseases: 42
Disease: Autistic Disorder ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Autistic Disorder
CUI: C0004352
Disease: Autistic Disorder
0.020 GeneticVariation BEFREE A common variant (rs53576, G/A) in the oxytocin receptor (OXTR) gene is associated with individual differences in social behavior and may increase the risk for neuropsychiatric disorders characterized by social impairment, especially autism. 31587084 2019
Autistic Disorder
CUI: C0004352
Disease: Autistic Disorder
0.020 GeneticVariation BEFREE When haplotypes were constructed with two, three, and four markers, the haplotype-specific FBAT revealed that a number of haplotypes, particularly those involving rs5357</span>6, were significantly associated with autism. 15992526 2005