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: rs111033437
rs111033437
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A
CUI: C0018784
Disease:
Sensorineural Hearing Loss (disorder)
A 0.700 GeneticVariation CLINVAR