Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs771827120
rs771827120
Entrez Id: 26047;105375554
Gene Symbol: CNTNAP2;LOC105375554
CNTNAP2;LOC105375554
CUI: C2750246
Disease:
Pitt-Hopkins-Like Syndrome 1
C 0.700 CausalMutation CLINVAR