Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs130065
rs130065
Entrez Id: 54535
Gene Symbol: CCHCR1
CCHCR1
CUI: C0042900
Disease:
Vitiligo 		0.700 GeneticVariation GWASDB Genome-wide association study for vitiligo identifies susceptibility loci at 6q27 and the MHC. 20526339 2010
dbSNP: rs130067
rs130067
Entrez Id: 54535
Gene Symbol: CCHCR1
CCHCR1
CUI: C0003873
Disease:
Rheumatoid Arthritis 		0.700 GeneticVariation GWASDB TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study. 17804836 2007
dbSNP: rs130067
rs130067
Entrez Id: 54535
Gene Symbol: CCHCR1
CCHCR1
CUI: C0376358
Disease:
Malignant neoplasm of prostate 		G 0.700 GeneticVariation GWASDB Seven prostate cancer susceptibility loci identified by a multi-stage genome-wide association study. 21743467 2011
dbSNP: rs130067
rs130067
Entrez Id: 54535
Gene Symbol: CCHCR1
CCHCR1
CUI: C0003873
Disease:
Rheumatoid Arthritis 		0.700 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
dbSNP: rs130072
rs130072
Entrez Id: 54535
Gene Symbol: CCHCR1
CCHCR1
CUI: C1836233
Disease:
AIDS, PROGRESSION TO 		0.700 GeneticVariation GWASDB The major genetic determinants of HIV-1 control affect HLA class I peptide presentation. 21051598 2010
dbSNP: rs130072
rs130072
Entrez Id: 54535
Gene Symbol: CCHCR1
CCHCR1
CUI: C1836230
Disease:
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO 		0.700 GeneticVariation GWASDB The major genetic determinants of HIV-1 control affect HLA class I peptide presentation. 21051598 2010
dbSNP: rs130072
rs130072
Entrez Id: 54535
Gene Symbol: CCHCR1
CCHCR1
CUI: C1836232
Disease:
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		0.700 GeneticVariation GWASDB The major genetic determinants of HIV-1 control affect HLA class I peptide presentation. 21051598 2010
dbSNP: rs130072
rs130072
Entrez Id: 54535
Gene Symbol: CCHCR1
CCHCR1
CUI: C1836231
Disease:
HIV-1, RESISTANCE TO 		0.700 GeneticVariation GWASDB The major genetic determinants of HIV-1 control affect HLA class I peptide presentation. 21051598 2010
dbSNP: rs130078
rs130078
Entrez Id: 54535
Gene Symbol: CCHCR1
CCHCR1
CUI: C0018213
Disease:
Graves Disease 		0.700 GeneticVariation GWASDB Identification of independent risk loci for Graves' disease within the MHC in the Japanese population. 21900946 2011
dbSNP: rs2073716
rs2073716
Entrez Id: 54535
Gene Symbol: CCHCR1
CCHCR1
CUI: C0004943
Disease:
Behcet Syndrome 		0.700 GeneticVariation GWASDB Identification of a susceptibility locus in STAT4 for Behçet's disease in Han Chinese in a genome-wide association study. 23001997 2012
dbSNP: rs2240064
rs2240064
Entrez Id: 54535
Gene Symbol: CCHCR1
CCHCR1
CUI: C0019829
Disease:
Hodgkin Disease 		G 0.700 GeneticVariation GWASDB Variation at 3p24.1 and 6q23.3 influences the risk of Hodgkin's lymphoma. 24149102 2013
dbSNP: rs3094187
rs3094187
Entrez Id: 6941;54535
Gene Symbol: TCF19;CCHCR1
TCF19;CCHCR1
CUI: C1836230
Disease:
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO 		0.700 GeneticVariation GWASDB Common genetic variation and the control of HIV-1 in humans. 20041166 2009
dbSNP: rs3094187
rs3094187
Entrez Id: 6941;54535
Gene Symbol: TCF19;CCHCR1
TCF19;CCHCR1
CUI: C1836232
Disease:
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		0.700 GeneticVariation GWASDB Common genetic variation and the control of HIV-1 in humans. 20041166 2009
dbSNP: rs3094187
rs3094187
Entrez Id: 6941;54535
Gene Symbol: TCF19;CCHCR1
TCF19;CCHCR1
CUI: C0018213
Disease:
Graves Disease 		0.700 GeneticVariation GWASDB Identification of independent risk loci for Graves' disease within the MHC in the Japanese population. 21900946 2011
dbSNP: rs3094187
rs3094187
Entrez Id: 6941;54535
Gene Symbol: TCF19;CCHCR1
TCF19;CCHCR1
CUI: C1836231
Disease:
HIV-1, RESISTANCE TO 		0.700 GeneticVariation GWASDB Common genetic variation and the control of HIV-1 in humans. 20041166 2009
dbSNP: rs3094187
rs3094187
Entrez Id: 6941;54535
Gene Symbol: TCF19;CCHCR1
TCF19;CCHCR1
CUI: C1836233
Disease:
AIDS, PROGRESSION TO 		0.700 GeneticVariation GWASDB Common genetic variation and the control of HIV-1 in humans. 20041166 2009
dbSNP: rs3130453
rs3130453
Entrez Id: 6941;54535
Gene Symbol: TCF19;CCHCR1
TCF19;CCHCR1
CUI: C1836230
Disease:
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO 		0.700 GeneticVariation GWASDB The major genetic determinants of HIV-1 control affect HLA class I peptide presentation. 21051598 2010
dbSNP: rs3130453
rs3130453
Entrez Id: 6941;54535
Gene Symbol: TCF19;CCHCR1
TCF19;CCHCR1
CUI: C1836231
Disease:
HIV-1, RESISTANCE TO 		0.700 GeneticVariation GWASDB The major genetic determinants of HIV-1 control affect HLA class I peptide presentation. 21051598 2010
dbSNP: rs3130453
rs3130453
Entrez Id: 6941;54535
Gene Symbol: TCF19;CCHCR1
TCF19;CCHCR1
CUI: C1836232
Disease:
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		0.700 GeneticVariation GWASDB The major genetic determinants of HIV-1 control affect HLA class I peptide presentation. 21051598 2010
dbSNP: rs3130453
rs3130453
Entrez Id: 6941;54535
Gene Symbol: TCF19;CCHCR1
TCF19;CCHCR1
CUI: C1836233
Disease:
AIDS, PROGRESSION TO 		0.700 GeneticVariation GWASDB The major genetic determinants of HIV-1 control affect HLA class I peptide presentation. 21051598 2010
dbSNP: rs3130455
rs3130455
Entrez Id: 6941;54535
Gene Symbol: TCF19;CCHCR1
TCF19;CCHCR1
CUI: C0042900
Disease:
Vitiligo 		0.700 GeneticVariation GWASDB Genome-wide association study for vitiligo identifies susceptibility loci at 6q27 and the MHC. 20526339 2010
dbSNP: rs720465
rs720465
Entrez Id: 6941;54535
Gene Symbol: TCF19;CCHCR1
TCF19;CCHCR1
CUI: C1836233
Disease:
AIDS, PROGRESSION TO 		0.700 GeneticVariation GWASDB Common genetic variation and the control of HIV-1 in humans. 20041166 2009
dbSNP: rs720465
rs720465
Entrez Id: 6941;54535
Gene Symbol: TCF19;CCHCR1
TCF19;CCHCR1
CUI: C1836232
Disease:
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		0.700 GeneticVariation GWASDB Common genetic variation and the control of HIV-1 in humans. 20041166 2009
dbSNP: rs720465
rs720465
Entrez Id: 6941;54535
Gene Symbol: TCF19;CCHCR1
TCF19;CCHCR1
CUI: C1836230
Disease:
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO 		0.700 GeneticVariation GWASDB Common genetic variation and the control of HIV-1 in humans. 20041166 2009
dbSNP: rs720465
rs720465
Entrez Id: 6941;54535
Gene Symbol: TCF19;CCHCR1
TCF19;CCHCR1
CUI: C1836230
Disease:
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO 		0.700 GeneticVariation GWASDB The major genetic determinants of HIV-1 control affect HLA class I peptide presentation. 21051598 2010