Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104893900
rs104893900
NKX2-5
0.010 GeneticVariation BEFREE We found one previously documented NKX2-5 missense mutation, T178M, in members of a family with ASD without AV conduction block. 12798584

2003