TYR, tyrosinase, 7299

N. diseases: 281; N. variants: 121
Disease: Hypopigmentation disorder ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs28940877
rs28940877
Entrez Id: 7299;107984363
Gene Symbol: TYR;LOC107984363
TYR;LOC107984363
CUI: C0162835
Disease:
Hypopigmentation disorder 		C 0.700 CausalMutation CLINVAR