Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1800561
rs1800561
CD38
0.020 GeneticVariation BEFREE The plasma levels of OXT in ASD subjects with the R140W allele were lower than those in ASD subjects lacking this allele. 22366648

2012
dbSNP: rs1800561
rs1800561
CD38
0.020 GeneticVariation BEFREE A mutation that caused tryptophan to replace arginine at amino acid residue 140 (R140W; (rs1800561, 4693C>T)) was found in 0.6-4.6% of the Japanese population and was associated with ASD in the smaller case-control study. 20435366

2010