Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2285803
rs2285803
Entrez Id: 170679;170680
Gene Symbol: PSORS1C1;PSORS1C2
PSORS1C1;PSORS1C2
CUI: C0026764
Disease:
Multiple Myeloma
0.810 GeneticVariation BEFREE Common single-nucleotide polymorphisms (SNPs) at 2p23.3 (rs6746082), 3p22.1 (rs1052501), 3q26.2 (rs10936599), 6p21.33 (rs2285803), 7p15.3 (rs4487645), 17p11.2 (rs4273077), and 22q13.1 (rs877529) have recently been shown to influence MM risk. 24449210 2014
dbSNP: rs2285803
rs2285803
Entrez Id: 170679;170680
Gene Symbol: PSORS1C1;PSORS1C2
PSORS1C1;PSORS1C2
CUI: C0026764
Disease:
Multiple Myeloma
A 0.810 GeneticVariation GWASDB Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk. 23955597 2013
dbSNP: rs2285803
rs2285803
Entrez Id: 170679;170680
Gene Symbol: PSORS1C1;PSORS1C2
PSORS1C1;PSORS1C2
CUI: C0026764
Disease:
Multiple Myeloma
A 0.810 GeneticVariation GWASCAT Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk. 23955597 2013
dbSNP: rs4959053
rs4959053
Entrez Id: 170679
Gene Symbol: PSORS1C1
PSORS1C1
CUI: C0004943
Disease:
Behcet Syndrome
0.800 GeneticVariation GWASDB Genome-wide association study identifies GIMAP as a novel susceptibility locus for Behcet's disease. 23041938 2013
dbSNP: rs4959053
rs4959053
Entrez Id: 170679
Gene Symbol: PSORS1C1
PSORS1C1
CUI: C0004943
Disease:
Behcet Syndrome
0.800 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: rs4959053
rs4959053
Entrez Id: 170679
Gene Symbol: PSORS1C1
PSORS1C1
CUI: C0004943
Disease:
Behcet Syndrome
0.800 GeneticVariation GWASCAT Identification of a susceptibility locus in STAT4 for Behçet's disease in Han Chinese in a genome-wide association study. 23001997 2012
dbSNP: rs3130573
rs3130573
Entrez Id: 170679;170680
Gene Symbol: PSORS1C1;PSORS1C2
PSORS1C1;PSORS1C2
CUI: C0036421
Disease:
Systemic Scleroderma
G 0.800 GeneticVariation GWASCAT Genome-wide scan identifies TNIP1, PSORS1C1, and RHOB as novel risk loci for systemic sclerosis. 21750679 2011
dbSNP: rs3130573
rs3130573
Entrez Id: 170679;170680
Gene Symbol: PSORS1C1;PSORS1C2
PSORS1C1;PSORS1C2
CUI: C0036421
Disease:
Systemic Scleroderma
G 0.800 GeneticVariation GWASDB Genome-wide scan identifies TNIP1, PSORS1C1, and RHOB as novel risk loci for systemic sclerosis. 21750679 2011
dbSNP: rs3815087
rs3815087
Entrez Id: 170679
Gene Symbol: PSORS1C1
PSORS1C1
CUI: C0038325
Disease:
Stevens-Johnson Syndrome
A 0.800 GeneticVariation GWASCAT Genome-wide association study of Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis in Europe. 21801394 2011
dbSNP: rs3815087
rs3815087
Entrez Id: 170679
Gene Symbol: PSORS1C1
PSORS1C1
CUI: C0038325
Disease:
Stevens-Johnson Syndrome
A 0.800 GeneticVariation GWASDB Genome-wide association study of Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis in Europe. 21801394 2011
dbSNP: rs3815087
rs3815087
Entrez Id: 170679
Gene Symbol: PSORS1C1
PSORS1C1
CUI: C1836230
Disease:
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
0.800 GeneticVariation GWASDB The major genetic determinants of HIV-1 control affect HLA class I peptide presentation. 21051598 2010
dbSNP: rs3815087
rs3815087
Entrez Id: 170679
Gene Symbol: PSORS1C1
PSORS1C1
CUI: C1836231
Disease:
HIV-1, RESISTANCE TO
0.800 GeneticVariation GWASDB The major genetic determinants of HIV-1 control affect HLA class I peptide presentation. 21051598 2010
dbSNP: rs3815087
rs3815087
Entrez Id: 170679
Gene Symbol: PSORS1C1
PSORS1C1
CUI: C1836233
Disease:
AIDS, PROGRESSION TO
0.800 GeneticVariation GWASDB The major genetic determinants of HIV-1 control affect HLA class I peptide presentation. 21051598 2010
dbSNP: rs3815087
rs3815087
Entrez Id: 170679
Gene Symbol: PSORS1C1
PSORS1C1
CUI: C1836232
Disease:
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
0.800 GeneticVariation GWASDB The major genetic determinants of HIV-1 control affect HLA class I peptide presentation. 21051598 2010
dbSNP: rs3815087
rs3815087
Entrez Id: 170679
Gene Symbol: PSORS1C1
PSORS1C1
CUI: C1836233
Disease:
AIDS, PROGRESSION TO
0.800 GeneticVariation GWASDB Common genetic variation and the control of HIV-1 in humans. 20041166 2009
dbSNP: rs3815087
rs3815087
Entrez Id: 170679
Gene Symbol: PSORS1C1
PSORS1C1
CUI: C1836231
Disease:
HIV-1, RESISTANCE TO
0.800 GeneticVariation GWASDB Common genetic variation and the control of HIV-1 in humans. 20041166 2009
dbSNP: rs3815087
rs3815087
Entrez Id: 170679
Gene Symbol: PSORS1C1
PSORS1C1
CUI: C1836231
Disease:
HIV-1, RESISTANCE TO
0.800 GeneticVariation GWASCAT Common genetic variation and the control of HIV-1 in humans. 20041166 2009
dbSNP: rs3815087
rs3815087
Entrez Id: 170679
Gene Symbol: PSORS1C1
PSORS1C1
CUI: C1836230
Disease:
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
0.800 GeneticVariation GWASDB Common genetic variation and the control of HIV-1 in humans. 20041166 2009
dbSNP: rs3815087
rs3815087
Entrez Id: 170679
Gene Symbol: PSORS1C1
PSORS1C1
CUI: C1836232
Disease:
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
0.800 GeneticVariation GWASCAT Common genetic variation and the control of HIV-1 in humans. 20041166 2009
dbSNP: rs3815087
rs3815087
Entrez Id: 170679
Gene Symbol: PSORS1C1
PSORS1C1
CUI: C1836233
Disease:
AIDS, PROGRESSION TO
0.800 GeneticVariation GWASCAT Common genetic variation and the control of HIV-1 in humans. 20041166 2009
dbSNP: rs3815087
rs3815087
Entrez Id: 170679
Gene Symbol: PSORS1C1
PSORS1C1
CUI: C1836230
Disease:
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
0.800 GeneticVariation GWASCAT Common genetic variation and the control of HIV-1 in humans. 20041166 2009
dbSNP: rs3815087
rs3815087
Entrez Id: 170679
Gene Symbol: PSORS1C1
PSORS1C1
CUI: C1836232
Disease:
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
0.800 GeneticVariation GWASDB Common genetic variation and the control of HIV-1 in humans. 20041166 2009
dbSNP: rs1265097
rs1265097
Entrez Id: 170679;170680
Gene Symbol: PSORS1C1;PSORS1C2
PSORS1C1;PSORS1C2
CUI: C0005890
Disease:
Body Height
0.700 GeneticVariation GWASCAT Genetic analyses of diverse populations improves discovery for complex traits. 31217584 2019
dbSNP: rs1265099
rs1265099
Entrez Id: 170679;170680
Gene Symbol: PSORS1C1;PSORS1C2
PSORS1C1;PSORS1C2
CUI: C1269683
Disease:
Major Depressive Disorder
A 0.700 GeneticVariation GWASCAT Bivariate genome-wide association analyses of the broad depression phenotype combined with major depressive disorder, bipolar disorder or schizophrenia reveal eight novel genetic loci for depression. 30626913 2019
dbSNP: rs1265099
rs1265099
Entrez Id: 170679;170680
Gene Symbol: PSORS1C1;PSORS1C2
PSORS1C1;PSORS1C2
CUI: C0036341
Disease:
Schizophrenia
A 0.700 GeneticVariation GWASCAT Bivariate genome-wide association analyses of the broad depression phenotype combined with major depressive disorder, bipolar disorder or schizophrenia reveal eight novel genetic loci for depression. 30626913 2019