PRKCB, protein kinase C beta, 5579

N. diseases: 317; N. variants: 18
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs7404095
rs7404095
Entrez Id: 5579
Gene Symbol: PRKCB
PRKCB
CUI: C0021390
Disease:
Inflammatory Bowel Diseases
0.800 GeneticVariation GWASCAT Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease. 28067908 2017
dbSNP: rs7404095
rs7404095
Entrez Id: 5579
Gene Symbol: PRKCB
PRKCB
CUI: C0021390
Disease:
Inflammatory Bowel Diseases
G 0.800 GeneticVariation GWASCAT Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations. 26192919 2015
dbSNP: rs7404095
rs7404095
Entrez Id: 5579
Gene Symbol: PRKCB
PRKCB
CUI: C0021390
Disease:
Inflammatory Bowel Diseases
C 0.800 GeneticVariation GWASCAT Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease. 23128233 2012
dbSNP: rs7404095
rs7404095
Entrez Id: 5579
Gene Symbol: PRKCB
PRKCB
CUI: C0021390
Disease:
Inflammatory Bowel Diseases
C 0.800 GeneticVariation GWASDB Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease. 23128233 2012
dbSNP: rs395897
rs395897
Entrez Id: 5579
Gene Symbol: PRKCB
PRKCB
CUI: C0596887
Disease:
mathematical ability
C 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs7404095
rs7404095
Entrez Id: 5579
Gene Symbol: PRKCB
PRKCB
CUI: C0009324
Disease:
Ulcerative Colitis
0.700 GeneticVariation GWASCAT Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease. 28067908 2017
dbSNP: rs7404928
rs7404928
Entrez Id: 5579
Gene Symbol: PRKCB
PRKCB
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: rs1131692056
rs1131692056
Entrez Id: 5579
Gene Symbol: PRKCB
PRKCB
CUI: C0018784
Disease:
Sensorineural Hearing Loss (disorder)
T 0.700 CausalMutation CLINVAR A novel missense variant in PRKCB segregates low-frequency hearing loss in an autosomal dominant family with Meniere's disease. 27329761 2016
dbSNP: rs7404095
rs7404095
Entrez Id: 5579
Gene Symbol: PRKCB
PRKCB
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: rs7404095
rs7404095
Entrez Id: 5579
Gene Symbol: PRKCB
PRKCB
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: rs7404095
rs7404095
Entrez Id: 5579
Gene Symbol: PRKCB
PRKCB
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: rs7404095
rs7404095
Entrez Id: 5579
Gene Symbol: PRKCB
PRKCB
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: rs7404095
rs7404095
Entrez Id: 5579
Gene Symbol: PRKCB
PRKCB
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
dbSNP: rs12921419
rs12921419
Entrez Id: 5579
Gene Symbol: PRKCB
PRKCB
CUI: C3548479
Disease:
response to bronchodilator
G 0.700 GeneticVariation GWASCAT A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry. 26634245 2015
dbSNP: rs12921419
rs12921419
Entrez Id: 5579
Gene Symbol: PRKCB
PRKCB
CUI: C0024117
Disease:
Chronic Obstructive Airway Disease
G 0.700 GeneticVariation GWASCAT A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry. 26634245 2015
dbSNP: rs12929627
rs12929627
Entrez Id: 5579
Gene Symbol: PRKCB
PRKCB
CUI: C3548479
Disease:
response to bronchodilator
T 0.700 GeneticVariation GWASCAT A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry. 26634245 2015
dbSNP: rs12929627
rs12929627
Entrez Id: 5579
Gene Symbol: PRKCB
PRKCB
CUI: C0024117
Disease:
Chronic Obstructive Airway Disease
T 0.700 GeneticVariation GWASCAT A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry. 26634245 2015
dbSNP: rs34289708
rs34289708
Entrez Id: 5579
Gene Symbol: PRKCB
PRKCB
CUI: C0024117
Disease:
Chronic Obstructive Airway Disease
C 0.700 GeneticVariation GWASCAT A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry. 26634245 2015
dbSNP: rs34289708
rs34289708
Entrez Id: 5579
Gene Symbol: PRKCB
PRKCB
CUI: C3548479
Disease:
response to bronchodilator
C 0.700 GeneticVariation GWASCAT A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry. 26634245 2015
dbSNP: rs35526040
rs35526040
Entrez Id: 5579
Gene Symbol: PRKCB
PRKCB
CUI: C0024117
Disease:
Chronic Obstructive Airway Disease
T 0.700 GeneticVariation GWASCAT A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry. 26634245 2015
dbSNP: rs35526040
rs35526040
Entrez Id: 5579
Gene Symbol: PRKCB
PRKCB
CUI: C3548479
Disease:
response to bronchodilator
T 0.700 GeneticVariation GWASCAT A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry. 26634245 2015
dbSNP: rs7404095
rs7404095
Entrez Id: 5579
Gene Symbol: PRKCB
PRKCB
CUI: C0009324
Disease:
Ulcerative Colitis
G 0.700 GeneticVariation GWASCAT Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations. 26192919 2015
dbSNP: rs9928486
rs9928486
Entrez Id: 5579
Gene Symbol: PRKCB
PRKCB
CUI: C3548479
Disease:
response to bronchodilator
C 0.700 GeneticVariation GWASCAT A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry. 26634245 2015
dbSNP: rs9928486
rs9928486
Entrez Id: 5579
Gene Symbol: PRKCB
PRKCB
CUI: C0024117
Disease:
Chronic Obstructive Airway Disease
C 0.700 GeneticVariation GWASCAT A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry. 26634245 2015
dbSNP: rs8059889
rs8059889
Entrez Id: 5579
Gene Symbol: PRKCB
PRKCB
CUI: C1445957
Disease:
Serum total cholesterol measurement
0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012