MYO15A, myosin XVA, 51168

N. diseases: 26; N. variants: 77
Disease: Deafness, Autosomal Recessive 3 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs765468034
rs765468034
Entrez Id: 51168;105371566
Gene Symbol: MYO15A;LOC105371566
MYO15A;LOC105371566
CUI: C1838263
Disease:
Deafness, Autosomal Recessive 3 		T 0.700 CausalMutation CLINVAR