MYO15A, myosin XVA, 51168

N. diseases: 26; N. variants: 77
Disease: Deafness, Autosomal Recessive 3 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1567658710
rs1567658710
Entrez Id: 51168
Gene Symbol: MYO15A
MYO15A
CUI: C1838263
Disease:
Deafness, Autosomal Recessive 3 		T 0.700 GeneticVariation CLINVAR