TYR, tyrosinase, 7299

N. diseases: 281; N. variants: 121
Disease: Albinism ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs61754388
rs61754388
Entrez Id: 7299;107984363
Gene Symbol: TYR;LOC107984363
TYR;LOC107984363
CUI: C0001916
Disease:
Albinism 		0.010 GeneticVariation BEFREE Functional validation of the albinism-associated tyrosinase T373K SNP by CRISPR/Cas9-mediated homology-directed repair (HDR) in rabbits. 30274819 2018