MYO5A, myosin VA, 4644

N. diseases: 82; N. variants: 4
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs764371254
rs764371254
Entrez Id: 4644
Gene Symbol: MYO5A
MYO5A
CUI: C1859194
Disease:
GRISCELLI SYNDROME, TYPE 1
A 0.700 CausalMutation CLINVAR
dbSNP: rs769021352
rs769021352
Entrez Id: 4644
Gene Symbol: MYO5A
MYO5A
CUI: C1859194
Disease:
GRISCELLI SYNDROME, TYPE 1
A 0.700 CausalMutation CLINVAR