TYR, tyrosinase, 7299

N. diseases: 281; N. variants: 121
Disease: melanoma ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1393350
rs1393350
Entrez Id: 7299;107984363
Gene Symbol: TYR;LOC107984363
TYR;LOC107984363
CUI: C0025202
Disease:
melanoma 		A 0.800 GeneticVariation GWASCAT Two-stage genome-wide association study identifies a novel susceptibility locus associated with melanoma. 28212542 2017
dbSNP: rs1393350
rs1393350
Entrez Id: 7299;107984363
Gene Symbol: TYR;LOC107984363
TYR;LOC107984363
CUI: C0025202
Disease:
melanoma 		0.800 GeneticVariation GWASDB A unique genome-wide association analysis in extended Utah high-risk pedigrees identifies a novel melanoma risk variant on chromosome arm 10q. 21706340 2012
dbSNP: rs1393350
rs1393350
Entrez Id: 7299;107984363
Gene Symbol: TYR;LOC107984363
TYR;LOC107984363
CUI: C0025202
Disease:
melanoma 		A 0.800 GeneticVariation GWASDB Genome-wide association study identifies three new melanoma susceptibility loci. 21983787 2011
dbSNP: rs1393350
rs1393350
Entrez Id: 7299;107984363
Gene Symbol: TYR;LOC107984363
TYR;LOC107984363
CUI: C0025202
Disease:
melanoma 		A 0.800 GeneticVariation GWASCAT Genome-wide association study identifies three new melanoma susceptibility loci. 21983787 2011
dbSNP: rs1393350
rs1393350
Entrez Id: 7299;107984363
Gene Symbol: TYR;LOC107984363
TYR;LOC107984363
CUI: C0025202
Disease:
melanoma 		A 0.800 GeneticVariation GWASDB Genome-wide association study identifies three loci associated with melanoma risk. 19578364 2009
dbSNP: rs1393350
rs1393350
Entrez Id: 7299;107984363
Gene Symbol: TYR;LOC107984363
TYR;LOC107984363
CUI: C0025202
Disease:
melanoma 		A 0.800 GeneticVariation GWASCAT Genome-wide association study identifies three loci associated with melanoma risk. 19578364 2009