MYO3A, myosin IIIA, 53904

N. diseases: 11; N. variants: 10
Disease: hearing impairment ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1564544199
rs1564544199
Entrez Id: 53904
Gene Symbol: MYO3A
MYO3A
CUI: C1384666
Disease:
hearing impairment 		T 0.700 CausalMutation CLINVAR