NFKB1, nuclear factor kappa B subunit 1, 4790

N. diseases: 551; N. variants: 52
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3774959
rs3774959
Entrez Id: 4790
Gene Symbol: NFKB1
NFKB1
CUI: C0009324
Disease:
Ulcerative Colitis 		A 0.800 GeneticVariation GWASCAT Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease. 23128233 2012
dbSNP: rs3774959
rs3774959
Entrez Id: 4790
Gene Symbol: NFKB1
NFKB1
CUI: C0009324
Disease:
Ulcerative Colitis 		A 0.800 GeneticVariation GWASDB Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease. 23128233 2012
dbSNP: rs113473633
rs113473633
Entrez Id: 4790
Gene Symbol: NFKB1
NFKB1
CUI: C0200638
Disease:
Eosinophil count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs113473633
rs113473633
Entrez Id: 4790
Gene Symbol: NFKB1
NFKB1
CUI: C0020676
Disease:
Hypothyroidism 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs113473633
rs113473633
Entrez Id: 4790
Gene Symbol: NFKB1
NFKB1
CUI: C0023508
Disease:
White Blood Cell Count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs230504
rs230504
Entrez Id: 4790
Gene Symbol: NFKB1
NFKB1
CUI: C0013595
Disease:
Eczema 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs230525
rs230525
Entrez Id: 4790
Gene Symbol: NFKB1
NFKB1
CUI: C0014772
Disease:
Red Blood Cell Count measurement 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs230534
rs230534
Entrez Id: 4790
Gene Symbol: NFKB1
NFKB1
CUI: C0036421
Disease:
Systemic Scleroderma 		T 0.700 GeneticVariation GWASCAT GWAS for systemic sclerosis identifies multiple risk loci and highlights fibrotic and vasculopathy pathways. 31672989 2019
dbSNP: rs4648133
rs4648133
Entrez Id: 4790;105377347
Gene Symbol: NFKB1;LOC105377347
NFKB1;LOC105377347
CUI: C0036421
Disease:
Systemic Scleroderma 		C 0.700 GeneticVariation GWASCAT Analysis of the genetic component of systemic sclerosis in Iranian and Turkish populations through a genome-wide association study. 30247649 2019
dbSNP: rs4699030
rs4699030
Entrez Id: 4790
Gene Symbol: NFKB1
NFKB1
CUI: C0149745
Disease:
Oral Ulcer 		C 0.700 GeneticVariation GWASCAT Genome wide analysis for mouth ulcers identifies associations at immune regulatory loci. 30837455 2019
dbSNP: rs12509403
rs12509403
Entrez Id: 4790;105377347
Gene Symbol: NFKB1;LOC105377347
NFKB1;LOC105377347
CUI: C2607914
Disease:
Allergic rhinitis (disorder) 		C 0.700 GeneticVariation GWASCAT Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis. 30013184 2018
dbSNP: rs151134704
rs151134704
Entrez Id: 4790;105377347
Gene Symbol: NFKB1;LOC105377347
NFKB1;LOC105377347
CUI: C0201976
Disease:
Creatinine measurement, serum (procedure) 		0.700 GeneticVariation GWASCAT Identification of CDC42BPG as a novel susceptibility locus for hyperuricemia in a Japanese population. 29124443 2018
dbSNP: rs151134704
rs151134704
Entrez Id: 4790;105377347
Gene Symbol: NFKB1;LOC105377347
NFKB1;LOC105377347
CUI: C0202239
Disease:
Uric acid measurement (procedure) 		0.700 GeneticVariation GWASCAT Identification of CDC42BPG as a novel susceptibility locus for hyperuricemia in a Japanese population. 29124443 2018
dbSNP: rs151134704
rs151134704
Entrez Id: 4790;105377347
Gene Symbol: NFKB1;LOC105377347
NFKB1;LOC105377347
CUI: C0017654
Disease:
Glomerular Filtration Rate 		0.700 GeneticVariation GWASCAT Identification of CDC42BPG as a novel susceptibility locus for hyperuricemia in a Japanese population. 29124443 2018
dbSNP: rs773694113
rs773694113
Entrez Id: 4790
Gene Symbol: NFKB1
NFKB1
CUI: C4225277
Disease:
IMMUNODEFICIENCY, COMMON VARIABLE, 12 		AT 0.700 CausalMutation CLINVAR Clinical efficacy of a next-generation sequencing gene panel for primary immunodeficiency diagnostics. 29077208 2018
dbSNP: rs1598856
rs1598856
Entrez Id: 4790
Gene Symbol: NFKB1
NFKB1
CUI: C0008312
Disease:
Primary biliary cirrhosis 		G 0.700 GeneticVariation GWASCAT A genome-wide association study identifies six novel risk loci for primary biliary cholangitis. 28425483 2017
dbSNP: rs230534
rs230534
Entrez Id: 4790
Gene Symbol: NFKB1
NFKB1
CUI: C0008312
Disease:
Primary biliary cirrhosis 		T 0.700 GeneticVariation GWASCAT Genome-wide association studies identify PRKCB as a novel genetic susceptibility locus for primary biliary cholangitis in the Japanese population. 28062665 2017
dbSNP: rs371681307
rs371681307
Entrez Id: 4790;105377347
Gene Symbol: NFKB1;LOC105377347
NFKB1;LOC105377347
CUI: C0008810
Disease:
Circadian Rhythms 		T 0.700 GeneticVariation GWASCAT Genome-wide association analysis of insomnia complaints identifies risk genes and genetic overlap with psychiatric and metabolic traits. 28604731 2017
dbSNP: rs113473633
rs113473633
Entrez Id: 4790
Gene Symbol: NFKB1
NFKB1
CUI: C0200638
Disease:
Eosinophil count procedure 		G 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs113473633
rs113473633
Entrez Id: 4790
Gene Symbol: NFKB1
NFKB1
CUI: C0200641
Disease:
Blood basophil count (lab test) 		G 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs3774937
rs3774937
Entrez Id: 4790
Gene Symbol: NFKB1
NFKB1
CUI: C0008313
Disease:
Cholangitis, Sclerosing 		0.700 GeneticVariation GWASCAT Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci. 26974007 2016
dbSNP: rs3774937
rs3774937
Entrez Id: 4790
Gene Symbol: NFKB1
NFKB1
CUI: C0033860
Disease:
Psoriasis 		0.700 GeneticVariation GWASCAT Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci. 26974007 2016
dbSNP: rs3774937
rs3774937
Entrez Id: 4790
Gene Symbol: NFKB1
NFKB1
CUI: C0038013
Disease:
Ankylosing spondylitis 		0.700 GeneticVariation GWASCAT Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci. 26974007 2016
dbSNP: rs3774937
rs3774937
Entrez Id: 4790
Gene Symbol: NFKB1
NFKB1
CUI: C0010346
Disease:
Crohn Disease 		0.700 GeneticVariation GWASCAT Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci. 26974007 2016
dbSNP: rs3774937
rs3774937
Entrez Id: 4790
Gene Symbol: NFKB1
NFKB1
CUI: C0009324
Disease:
Ulcerative Colitis 		0.700 GeneticVariation GWASCAT Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci. 26974007 2016