NCOA5, nuclear receptor coactivator 5, 57727

N. diseases: 53; N. variants: 5
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2425752
rs2425752
Entrez Id: 57727
Gene Symbol: NCOA5
NCOA5
CUI: C0026769
Disease:
Multiple Sclerosis 		0.800 GeneticVariation GWASCAT Genetic overlap between autoimmune diseases and non-Hodgkin lymphoma subtypes. 31407831 2019
dbSNP: rs2425752
rs2425752
Entrez Id: 57727
Gene Symbol: NCOA5
NCOA5
CUI: C0026769
Disease:
Multiple Sclerosis 		A 0.800 GeneticVariation GWASDB Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. 21833088 2011
dbSNP: rs2425752
rs2425752
Entrez Id: 57727
Gene Symbol: NCOA5
NCOA5
CUI: C0026769
Disease:
Multiple Sclerosis 		A 0.800 GeneticVariation GWASCAT Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. 21833088 2011
dbSNP: rs2425752
rs2425752
Entrez Id: 57727
Gene Symbol: NCOA5
NCOA5
CUI: C0079744
Disease:
Diffuse Large B-Cell Lymphoma 		0.700 GeneticVariation GWASCAT Genetic overlap between autoimmune diseases and non-Hodgkin lymphoma subtypes. 31407831 2019
dbSNP: rs2425752
rs2425752
Entrez Id: 57727
Gene Symbol: NCOA5
NCOA5
CUI: C1367654
Disease:
Marginal Zone B-Cell Lymphoma 		0.700 GeneticVariation GWASCAT Genetic overlap between autoimmune diseases and non-Hodgkin lymphoma subtypes. 31407831 2019
dbSNP: rs6074015
rs6074015
Entrez Id: 57727
Gene Symbol: NCOA5
NCOA5
CUI: C0014772
Disease:
Red Blood Cell Count measurement 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs2425752
rs2425752
Entrez Id: 57727
Gene Symbol: NCOA5
NCOA5
CUI: C0019829
Disease:
Hodgkin Disease 		T 0.700 GeneticVariation GWASCAT We identify 5 new HL risk loci at 6p21.31 (rs649775; <i>P</i> = 2.11 × 10<sup>-10</sup>), 6q23.3 (rs1002658; <i>P</i> = 2.97 × 10<sup>-8</sup>), 11q23.1 (rs7111520; <i>P</i> = 1.44 × 10<sup>-11</sup>), 16p11.2 (rs6565176; <i>P</i> = 4.00 × 10<sup>-8</sup>), and 20q13.12 (rs2425752; <i>P</i> = 2.01 × 10<sup>-8</sup>). 30194254 2018
dbSNP: rs6074013
rs6074013
Entrez Id: 57727
Gene Symbol: NCOA5
NCOA5
CUI: C1269683
Disease:
Major Depressive Disorder 		0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways. 29942085 2018
dbSNP: rs6074013
rs6074013
Entrez Id: 57727
Gene Symbol: NCOA5
NCOA5
CUI: C0525045
Disease:
Mood Disorders 		0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways. 29942085 2018
dbSNP: rs17450969
rs17450969
Entrez Id: 57727
Gene Symbol: NCOA5
NCOA5
CUI: C2700366
Disease:
Adiponectin Measurement 		0.700 GeneticVariation GWASDB Adiponectin concentrations: a genome-wide association study. 20887962 2010
dbSNP: rs2903908
rs2903908
Entrez Id: 57727
Gene Symbol: NCOA5
NCOA5
CUI: C0004943
Disease:
Behcet Syndrome 		0.010 GeneticVariation BEFREE Our study represents for the first time that the <i>NCOA5</i> rs2903908 polymorphism seemed to be linked to BD susceptibility and clinical findings. 28694762 2017
dbSNP: rs2903908
rs2903908
Entrez Id: 57727
Gene Symbol: NCOA5
NCOA5
CUI: C0033860
Disease:
Psoriasis 		0.010 GeneticVariation BEFREE Alleles G and C of the CD40 rs4810485 and NCOA5 rs2903908 SNPs, respectively, were more common in individuals with PS than in controls (p = 0.03, odds ratio [OR] = 1.42, 95% confidence interval [95% CI] 1.05-1.95 and p = 0.000 003, OR = 1.93, 95% CI 1.47-2.55, respectively). 21645569 2011