Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1064797090
rs1064797090
Entrez Id: 2706
Gene Symbol: GJB2
GJB2
CUI: C2675750
Disease:
DEAFNESS, AUTOSOMAL DOMINANT 3A (disorder)
C 0.700 CausalMutation CLINVAR
dbSNP: rs1064797090
rs1064797090
Entrez Id: 2706
Gene Symbol: GJB2
GJB2
CUI: C2675750
Disease:
DEAFNESS, AUTOSOMAL DOMINANT 3A (disorder)
A 0.700 GeneticVariation CLINVAR