Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1569118680
rs1569118680
Entrez Id: 57502
Gene Symbol: NLGN4X
NLGN4X
CUI: C3501611
Disease:
Mental Retardation, X-Linked Nonsyndromic
G 0.700 CausalMutation CLINVAR