Disease: hearing impairment ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1445287184
rs1445287184
Entrez Id: 374462;105369867
Gene Symbol: PTPRQ;LOC105369867
PTPRQ;LOC105369867
CUI: C1384666
Disease:
hearing impairment 		T 0.700 CausalMutation CLINVAR