Disease: Deafness, Autosomal Dominant 2A ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1271250198
rs1271250198
Entrez Id: 9132
Gene Symbol: KCNQ4
KCNQ4
CUI: C2677637
Disease:
Deafness, Autosomal Dominant 2A 		C 0.700 CausalMutation CLINVAR