CSNK2B, casein kinase 2 beta, 1460

N. diseases: 34; N. variants: 6
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs9267531
rs9267531
Entrez Id: 1460;58496
Gene Symbol: CSNK2B;LY6G5B
CSNK2B;LY6G5B
CUI: C0024141
Disease:
Lupus Erythematosus, Systemic 		0.700 GeneticVariation GWASCAT Identification of a New Susceptibility Locus for Systemic Lupus Erythematosus on Chromosome 12 in Individuals of European Ancestry. 26316170 2016
dbSNP: rs9267531
rs9267531
Entrez Id: 1460;58496
Gene Symbol: CSNK2B;LY6G5B
CSNK2B;LY6G5B
CUI: C0024137
Disease:
Lupus Erythematosus, Cutaneous 		G 0.700 GeneticVariation GWASCAT Genome-wide association study identifies new susceptibility loci for cutaneous lupus erythematosus. 25827949 2015
dbSNP: rs3130618
rs3130618
Entrez Id: 1460;7918
Gene Symbol: CSNK2B;GPANK1
CSNK2B;GPANK1
CUI: C0024141
Disease:
Lupus Erythematosus, Systemic 		A 0.700 GeneticVariation GWASDB GWAS identifies novel SLE susceptibility genes and explains the association of the HLA region. 24871463 2014
dbSNP: rs3130618
rs3130618
Entrez Id: 1460;7918
Gene Symbol: CSNK2B;GPANK1
CSNK2B;GPANK1
CUI: C0149678
Disease:
Epstein-Barr Virus Infections 		0.700 GeneticVariation GWASDB A genome-wide integrative genomic study localizes genetic factors influencing antibodies against Epstein-Barr virus nuclear antigen 1 (EBNA-1). 23326239 2013
dbSNP: rs3130618
rs3130618
Entrez Id: 1460;7918
Gene Symbol: CSNK2B;GPANK1
CSNK2B;GPANK1
CUI: C0524587
Disease:
Mean Corpuscular Volume (result) 		0.700 GeneticVariation GWASDB Genome-wide association study of serum albumin:globulin ratio in Korean populations. 23303382 2013
dbSNP: rs9267532
rs9267532
Entrez Id: 1460;58496
Gene Symbol: CSNK2B;LY6G5B
CSNK2B;LY6G5B
CUI: C0149678
Disease:
Epstein-Barr Virus Infections 		0.700 GeneticVariation GWASDB A genome-wide integrative genomic study localizes genetic factors influencing antibodies against Epstein-Barr virus nuclear antigen 1 (EBNA-1). 23326239 2013
dbSNP: rs3130618
rs3130618
Entrez Id: 1460;7918
Gene Symbol: CSNK2B;GPANK1
CSNK2B;GPANK1
CUI: C0026896
Disease:
Myasthenia Gravis 		0.700 GeneticVariation GWASDB Risk for myasthenia gravis maps to a (151) Pro→Ala change in TNIP1 and to human leukocyte antigen-B*08. 23055271 2012
dbSNP: rs3117579
rs3117579
Entrez Id: 1460;7918
Gene Symbol: CSNK2B;GPANK1
CSNK2B;GPANK1
CUI: C0003873
Disease:
Rheumatoid Arthritis 		0.700 GeneticVariation GWASDB A genome-wide association study suggests contrasting associations in ACPA-positive versus ACPA-negative rheumatoid arthritis. 21156761 2011
dbSNP: rs3130618
rs3130618
Entrez Id: 1460;7918
Gene Symbol: CSNK2B;GPANK1
CSNK2B;GPANK1
CUI: C0017665
Disease:
Membranous glomerulonephritis 		A 0.700 GeneticVariation GWASCAT Risk HLA-DQA1 and PLA(2)R1 alleles in idiopathic membranous nephropathy. 21323541 2011
dbSNP: rs3130618
rs3130618
Entrez Id: 1460;7918
Gene Symbol: CSNK2B;GPANK1
CSNK2B;GPANK1
CUI: C0003873
Disease:
Rheumatoid Arthritis 		0.700 GeneticVariation GWASDB A genome-wide association study suggests contrasting associations in ACPA-positive versus ACPA-negative rheumatoid arthritis. 21156761 2011
dbSNP: rs707919
rs707919
Entrez Id: 1460;58496
Gene Symbol: CSNK2B;LY6G5B
CSNK2B;LY6G5B
CUI: C0003873
Disease:
Rheumatoid Arthritis 		0.700 GeneticVariation GWASDB A genome-wide association study suggests contrasting associations in ACPA-positive versus ACPA-negative rheumatoid arthritis. 21156761 2011
dbSNP: rs9267531
rs9267531
Entrez Id: 1460;58496
Gene Symbol: CSNK2B;LY6G5B
CSNK2B;LY6G5B
CUI: C0003873
Disease:
Rheumatoid Arthritis 		0.700 GeneticVariation GWASDB A genome-wide association study suggests contrasting associations in ACPA-positive versus ACPA-negative rheumatoid arthritis. 21156761 2011
dbSNP: rs3130618
rs3130618
Entrez Id: 1460;7918
Gene Symbol: CSNK2B;GPANK1
CSNK2B;GPANK1
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: rs3130618
rs3130618
Entrez Id: 1460;7918
Gene Symbol: CSNK2B;GPANK1
CSNK2B;GPANK1
CUI: C0011854
Disease:
Diabetes Mellitus, Insulin-Dependent 		0.700 GeneticVariation GWASDB A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene. 17632545 2007
dbSNP: rs3130618
rs3130618
Entrez Id: 1460;7918
Gene Symbol: CSNK2B;GPANK1
CSNK2B;GPANK1
CUI: C0003873
Disease:
Rheumatoid Arthritis 		0.700 GeneticVariation GWASDB TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study. 17804836 2007
dbSNP: rs9267532
rs9267532
Entrez Id: 1460;58496
Gene Symbol: CSNK2B;LY6G5B
CSNK2B;LY6G5B
CUI: C0011854
Disease:
Diabetes Mellitus, Insulin-Dependent 		0.700 GeneticVariation GWASDB A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene. 17632545 2007
dbSNP: rs1346452438
rs1346452438
Entrez Id: 1460;58496
Gene Symbol: CSNK2B;LY6G5B
CSNK2B;LY6G5B
CUI: C0038454
Disease:
Cerebrovascular accident 		0.010 GeneticVariation BEFREE The Val12Met SNP in ABCG2 was associated with stroke in both white (hazard ratio, 1.46; 90% CI, 1.05 to 2.03) and black (hazard ratio, 3.59; 90% CI, 1.11 to 11.6) participants of CHS. 19023099 2009
dbSNP: rs1346452438
rs1346452438
Entrez Id: 1460;58496
Gene Symbol: CSNK2B;LY6G5B
CSNK2B;LY6G5B
CUI: C0948008
Disease:
Ischemic stroke 		0.010 GeneticVariation BEFREE The Val12Met SNP in ABCG2 (encoding a transporter of sterols and xenobiotics) was associated with incident ischemic stroke in white and black participants of CHS. 19023099 2009