MYH9, myosin heavy chain 9, 4627

N. diseases: 196; N. variants: 38
Disease: Hypermelanotic macule ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1430793034
rs1430793034
Entrez Id: 4627
Gene Symbol: MYH9
MYH9
CUI: C1842774
Disease:
Hypermelanotic macule 		A 0.700 GeneticVariation CLINVAR