Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1565819402
rs1565819402
Entrez Id: 374462;105369867
Gene Symbol: PTPRQ;LOC105369867
PTPRQ;LOC105369867
CUI: C0011053
Disease:
Deafness
A 0.700 CausalMutation CLINVAR
dbSNP: rs1565855932
rs1565855932
Entrez Id: 374462;105369867
Gene Symbol: PTPRQ;LOC105369867
PTPRQ;LOC105369867
CUI: C0011053
Disease:
Deafness
A 0.700 CausalMutation CLINVAR