Source: GWASDB

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 54535
Gene Symbol: CCHCR1
CCHCR1
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		0.400 GeneticVariation GWASDB Seven prostate cancer susceptibility loci identified by a multi-stage genome-wide association study. 21743467

2011
Entrez Id: 54535
Gene Symbol: CCHCR1
CCHCR1
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease 		0.120 GeneticVariation GWASDB Variation at 3p24.1 and 6q23.3 influences the risk of Hodgkin's lymphoma. 24149102

2013
Entrez Id: 54535
Gene Symbol: CCHCR1
CCHCR1
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		0.110 GeneticVariation GWASDB A genome-wide association study identified new variants associated with the risk of chronic hepatitis B. 23760081

2013
Entrez Id: 54535
Gene Symbol: CCHCR1
CCHCR1
CUI: C0004096
Disease: Asthma
Asthma 		0.110 GeneticVariation GWASDB A large-scale, consortium-based genomewide association study of asthma. 20860503

2010
Entrez Id: 54535
Gene Symbol: CCHCR1
CCHCR1
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.100 GeneticVariation GWASDB Identification of a susceptibility locus in STAT4 for Behçet's disease in Han Chinese in a genome-wide association study. 23001997

2012
Entrez Id: 54535
Gene Symbol: CCHCR1
CCHCR1
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.100 GeneticVariation GWASDB Identification of independent risk loci for Graves' disease within the MHC in the Japanese population. 21900946

2011
Entrez Id: 54535
Gene Symbol: CCHCR1
CCHCR1
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.100 GeneticVariation GWASDB Genome-wide association study for vitiligo identifies susceptibility loci at 6q27 and the MHC. 20526339

2010
Entrez Id: 54535
Gene Symbol: CCHCR1
CCHCR1
CUI: C1836230
Disease: HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO 		0.100 GeneticVariation GWASDB The major genetic determinants of HIV-1 control affect HLA class I peptide presentation. 21051598

2010
Entrez Id: 54535
Gene Symbol: CCHCR1
CCHCR1
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO 		0.100 GeneticVariation GWASDB The major genetic determinants of HIV-1 control affect HLA class I peptide presentation. 21051598

2010
Entrez Id: 54535
Gene Symbol: CCHCR1
CCHCR1
CUI: C1836232
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		0.100 GeneticVariation GWASDB The major genetic determinants of HIV-1 control affect HLA class I peptide presentation. 21051598

2010
Entrez Id: 54535
Gene Symbol: CCHCR1
CCHCR1
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO 		0.100 GeneticVariation GWASDB The major genetic determinants of HIV-1 control affect HLA class I peptide presentation. 21051598

2010
Entrez Id: 54535
Gene Symbol: CCHCR1
CCHCR1
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.100 GeneticVariation GWASDB REL, encoding a member of the NF-kappaB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis. 19503088

2009
Entrez Id: 54535
Gene Symbol: CCHCR1
CCHCR1
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.100 GeneticVariation GWASDB A genome-wide association study identifies three new susceptibility loci for ulcerative colitis in the Japanese population. 19915573

2009
Entrez Id: 54535
Gene Symbol: CCHCR1
CCHCR1
CUI: C1836230
Disease: HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO 		0.100 GeneticVariation GWASDB Common genetic variation and the control of HIV-1 in humans. 20041166

2009
Entrez Id: 54535
Gene Symbol: CCHCR1
CCHCR1
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO 		0.100 GeneticVariation GWASDB Common genetic variation and the control of HIV-1 in humans. 20041166

2009
Entrez Id: 54535
Gene Symbol: CCHCR1
CCHCR1
CUI: C1836232
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		0.100 GeneticVariation GWASDB Common genetic variation and the control of HIV-1 in humans. 20041166

2009
Entrez Id: 54535
Gene Symbol: CCHCR1
CCHCR1
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO 		0.100 GeneticVariation GWASDB Common genetic variation and the control of HIV-1 in humans. 20041166

2009
Entrez Id: 54535
Gene Symbol: CCHCR1
CCHCR1
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.100 GeneticVariation GWASDB TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study. 17804836

2007