MYO7A, myosin VIIA, 4647

N. diseases: 104; N. variants: 194
Disease: hearing impairment ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1555076948
rs1555076948
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A
CUI: C1384666
Disease:
hearing impairment 		T 0.700 GeneticVariation CLINVAR