NCOA6, nuclear receptor coactivator 6, 23054

N. diseases: 64; N. variants: 36
Disease: melanoma ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4911442
rs4911442
Entrez Id: 23054
Gene Symbol: NCOA6
NCOA6
CUI: C0025202
Disease:
melanoma 		0.720 GeneticVariation 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
dbSNP: rs4911442
rs4911442
Entrez Id: 23054
Gene Symbol: NCOA6
NCOA6
CUI: C0025202
Disease:
melanoma 		0.720 GeneticVariation BEFREE Our data confirmed a previous association of melanoma risk (OR 1.82, 95% CI 1.37-2.41) with rs4911442, located in intron 5 of the nuclear receptor coactivator 6 (NCOA6) gene. 22628150 2013
dbSNP: rs4911442
rs4911442
Entrez Id: 23054
Gene Symbol: NCOA6
NCOA6
CUI: C0025202
Disease:
melanoma 		0.720 GeneticVariation GWASDB Common sequence variants on 20q11.22 confer melanoma susceptibility. 18488026 2008
dbSNP: rs7271289
rs7271289
Entrez Id: 23054
Gene Symbol: NCOA6
NCOA6
CUI: C0025202
Disease:
melanoma 		0.700 GeneticVariation GWASDB Common sequence variants on 20q11.22 confer melanoma susceptibility. 18488026 2008
dbSNP: rs910871
rs910871
Entrez Id: 23054
Gene Symbol: NCOA6
NCOA6
CUI: C0025202
Disease:
melanoma 		0.010 GeneticVariation BEFREE The rs910871, one of the six variants, genotyped to cover NCOA6, showed an association with melanoma risk (OR 1.33, 95% CI 1.04-1.70). 22628150 2013