Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs9263739
rs9263739
Entrez Id: 54535
Gene Symbol: CCHCR1
CCHCR1
CUI: C0009324
Disease:
Ulcerative Colitis 		T 0.800 GeneticVariation GWASCAT A genome-wide association study identifies three new susceptibility loci for ulcerative colitis in the Japanese population. 19915573 2009
dbSNP: rs9263739
rs9263739
Entrez Id: 54535
Gene Symbol: CCHCR1
CCHCR1
CUI: C0009324
Disease:
Ulcerative Colitis 		T 0.800 GeneticVariation GWASDB A genome-wide association study identifies three new susceptibility loci for ulcerative colitis in the Japanese population. 19915573 2009
dbSNP: rs1576
rs1576
Entrez Id: 54535
Gene Symbol: CCHCR1
CCHCR1
CUI: C0033860
Disease:
Psoriasis 		0.710 GeneticVariation GWASCAT Genome-wide association study of psoriasis in an Egyptian population. 30921485 2019
dbSNP: rs1576
rs1576
Entrez Id: 54535
Gene Symbol: CCHCR1
CCHCR1
CUI: C0033860
Disease:
Psoriasis 		0.710 GeneticVariation BEFREE The noncoding SNPs rs1265112 and rs746647 were in complete linkage disequilibrium with the nonsynonymous SNP rs1576 (r(2) = 1.00), which has been associated with psoriasis. 21810746 2011
dbSNP: rs115321690
rs115321690
Entrez Id: 54535
Gene Symbol: CCHCR1
CCHCR1
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent 		G 0.700 GeneticVariation GWASCAT Identification of 28 new susceptibility loci for type 2 diabetes in the Japanese population. 30718926 2019
dbSNP: rs2240060
rs2240060
Entrez Id: 54535
Gene Symbol: CCHCR1
CCHCR1
CUI: C0730345
Disease:
Microalbuminuria 		A 0.700 GeneticVariation GWASCAT Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria. 31511532 2019
dbSNP: rs130067
rs130067
Entrez Id: 54535
Gene Symbol: CCHCR1
CCHCR1
CUI: C0600139
Disease:
Prostate carcinoma 		G 0.700 GeneticVariation GWASCAT Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci. 29892016 2018
dbSNP: rs3132535
rs3132535
Entrez Id: 54535
Gene Symbol: CCHCR1
CCHCR1
CUI: C0026764
Disease:
Multiple Myeloma 		A 0.700 GeneticVariation GWASCAT Genome-wide association study identifies multiple susceptibility loci for multiple myeloma. 27363682 2016
dbSNP: rs1265115
rs1265115
Entrez Id: 54535
Gene Symbol: CCHCR1
CCHCR1
CUI: C0019163
Disease:
Hepatitis B 		0.700 GeneticVariation GWASDB A genome-wide association study identified new variants associated with the risk of chronic hepatitis B. 23760081 2013
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: 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: 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: C0600139
Disease:
Prostate carcinoma 		G 0.700 GeneticVariation GWASCAT Seven prostate cancer susceptibility loci identified by a multi-stage genome-wide association study. 21743467 2011
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: 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: rs1265115
rs1265115
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: rs1265115
rs1265115
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: rs1265115
rs1265115
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: rs1265115
rs1265115
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: rs130065
rs130065
Entrez Id: 54535
Gene Symbol: CCHCR1
CCHCR1
CUI: C0004096
Disease:
Asthma 		0.700 GeneticVariation GWASDB A large-scale, consortium-based genomewide association study of asthma. 20860503 2010
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: 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