Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
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: 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: rs805262
rs805262
Entrez Id: 7917;7918;57827
Gene Symbol: BAG6;GPANK1;C6orf47
BAG6;GPANK1;C6orf47
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: rs805262
rs805262
Entrez Id: 7917;7918;57827
Gene Symbol: BAG6;GPANK1;C6orf47
BAG6;GPANK1;C6orf47
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: rs805262
rs805262
Entrez Id: 7917;7918;57827
Gene Symbol: BAG6;GPANK1;C6orf47
BAG6;GPANK1;C6orf47
CUI: C0003873
Disease:
Rheumatoid Arthritis 		0.700 GeneticVariation GWASDB TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study. 17804836 2007
dbSNP: rs707974
rs707974
Entrez Id: 7917;7918;57827
Gene Symbol: BAG6;GPANK1;C6orf47
BAG6;GPANK1;C6orf47
CUI: C0034067
Disease:
Pulmonary Emphysema 		0.010 GeneticVariation BEFREE SNPs in a second gene related to apolipoprotein M and HDL, PCSK9, were associated with FEV1/FVC ratio among African-Americans. rs707974 was associated with per cent emphysema among European-Americans and African-Americans and APOM expression was related to FEV1/FVC ratio and per cent emphysema. 23900982 2014