Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs753669213
rs753669213
LBX2
0.010 GeneticVariation BEFREE A rare missense mutation in LBX2 (c.A403G: p.K135E) was identified as the pathogenic cause of ASD. 29669692

2018