MYO7A, myosin VIIA, 4647

N. diseases: 104; N. variants: 194
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1253943370
rs1253943370
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A
CUI: C3887873
Disease:
Hearing Loss
A 0.700 CausalMutation CLINVAR
dbSNP: rs782539587
rs782539587
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A
CUI: C3887873
Disease:
Hearing Loss
T 0.700 CausalMutation CLINVAR