TYR, tyrosinase, 7299

N. diseases: 281; N. variants: 121
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma
0.110 GeneticVariation disease GWASCAT Combined analysis of keratinocyte cancers identifies novel genome-wide loci. 31174203 2019
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma
0.110 GeneticVariation disease GWASCAT Identification of Susceptibility Loci for Cutaneous Squamous Cell Carcinoma. 26829030 2016
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma
0.110 GeneticVariation disease BEFREE The TYR haplotype carrying only the Arg402Gln variant allele was significantly associated with SCC risk (OR, 1.35; 95% CI, 1.04-1.74). 19384953 2009