NCOA6, nuclear receptor coactivator 6, 23054

N. diseases: 64; N. variants: 36
Disease: melanoma ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0025202
Disease: melanoma
melanoma 		0.120 GeneticVariation disease BEFREE In the PanScan data, initial associations were found with melanoma susceptibility variants in NCOA6 [rs4911442; OR, 1.32; 95% confidence interval (CI), 1.03-1.70; P = 0.03], YWHAZP5 (rs17119461; OR, 2.62; 95% CI, 1.08-6.35; P = 0.03), and YWHAZP5 (rs17119490; OR, 2.62; 95% CI, 1.08-6.34; P = 0.03), TYRP1 (P = 0.04), and IFNA13 (P = 0.04). 24642353 2014
CUI: C0025202
Disease: melanoma
melanoma 		0.120 GeneticVariation disease BEFREE A haplotype from the variants within NCOA6 showed an association with risk of melanoma (OR 1.49, 95% CI 1.17-1.88). 22628150 2013
CUI: C0025202
Disease: melanoma
melanoma 		0.120 GeneticVariation disease GWASDB Common sequence variants on 20q11.22 confer melanoma susceptibility. 18488026 2008