Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1042778
rs1042778
CAV3 ; OXTR
0.020 GeneticVariation BEFREE A genetic risk score was calculated based on four OXTR single nucleotide polymorphisms (rs53576, rs237887, rs1042778, and rs2254298) previously reported to be associated with ASD symptomatology. 31025834

2019
dbSNP: rs1042778
rs1042778
CAV3 ; OXTR
0.020 GeneticVariation BEFREE Also, in the family-based analysis, a trend towards association with ASD susceptibility was observed for rs1042778 (G allele) (P = 0.066). 29858823

2018