Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1126809
rs1126809
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma
0.710 GeneticVariation 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