MYH14, myosin heavy chain 14, 79784

N. diseases: 64; N. variants: 9
Disease: Deafness, Autosomal Dominant 4 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs119103281
rs119103281
Entrez Id: 79784
Gene Symbol: MYH14
MYH14
CUI: C1833503
Disease:
Deafness, Autosomal Dominant 4 		T 0.700 CausalMutation CLINVAR