Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs193024911
rs193024911
SYN2
0.010 GeneticVariation BEFREE In this study, we show that nonsense (A94fs199X) and missense (Y236S and G464R) mutations in SYN2 are associated with ASD in humans.The phenotype is apparent in males. 23956174

2014