CDC37, cell division cycle 37, 11140

N. diseases: 30; N. variants: 4
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11879191
rs11879191
Entrez Id: 11140
Gene Symbol: CDC37
CDC37
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: rs11879191
rs11879191
Entrez Id: 11140
Gene Symbol: CDC37
CDC37
CUI: C0021390
Disease:
Inflammatory Bowel Diseases 		G 0.800 GeneticVariation GWASDB Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease. 23128233 2012
dbSNP: rs11879191
rs11879191
Entrez Id: 11140
Gene Symbol: CDC37
CDC37
CUI: C0021390
Disease:
Inflammatory Bowel Diseases 		G 0.800 GeneticVariation GWASCAT Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease. 23128233 2012
dbSNP: rs8112449
rs8112449
Entrez Id: 11140
Gene Symbol: CDC37
CDC37
CUI: C0026769
Disease:
Multiple Sclerosis 		G 0.800 GeneticVariation GWASCAT Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. 21833088 2011
dbSNP: rs8112449
rs8112449
Entrez Id: 11140
Gene Symbol: CDC37
CDC37
CUI: C0026769
Disease:
Multiple Sclerosis 		G 0.800 GeneticVariation GWASDB Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. 21833088 2011
dbSNP: rs11879191
rs11879191
Entrez Id: 11140
Gene Symbol: CDC37
CDC37
CUI: C0010346
Disease:
Crohn Disease 		0.700 GeneticVariation GWASCAT Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease. 28067908 2017
dbSNP: rs11879191
rs11879191
Entrez Id: 11140
Gene Symbol: CDC37
CDC37
CUI: C0010346
Disease:
Crohn Disease 		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: rs35164067
rs35164067
Entrez Id: 11140
Gene Symbol: CDC37
CDC37
CUI: C0021390
Disease:
Inflammatory Bowel Diseases 		0.700 GeneticVariation GWASCAT Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations. 26192919 2015
dbSNP: rs35164067
rs35164067
Entrez Id: 11140
Gene Symbol: CDC37
CDC37
CUI: C0038013
Disease:
Ankylosing spondylitis 		G 0.700 GeneticVariation GWASCAT Identification of multiple risk variants for ankylosing spondylitis through high-density genotyping of immune-related loci. 23749187 2013
dbSNP: rs8112449
rs8112449
Entrez Id: 11140
Gene Symbol: CDC37
CDC37
CUI: C0020445
Disease:
Hypercholesterolemia, Familial 		0.700 GeneticVariation GWASDB Low-density lipoprotein receptor mutations generate synthetic genome-wide associations. 22968135 2013
dbSNP: rs553040076
rs553040076
Entrez Id: 5141;11140
Gene Symbol: PDE4A;CDC37
PDE4A;CDC37
CUI: C0344315
Disease:
Depressed mood 		0.010 GeneticVariation BEFREE Q31L mutants had lower PDE4B activity, consistent with their resistance to rolipram, suggesting decreased PDE4 activity as a contributory factor in depression. 17481393 2007
dbSNP: rs553040076
rs553040076
Entrez Id: 5141;11140
Gene Symbol: PDE4A;CDC37
PDE4A;CDC37
CUI: C0011570
Disease:
Mental Depression 		0.010 GeneticVariation BEFREE Q31L mutants had lower PDE4B activity, consistent with their resistance to rolipram, suggesting decreased PDE4 activity as a contributory factor in depression. 17481393 2007
dbSNP: rs553040076
rs553040076
Entrez Id: 5141;11140
Gene Symbol: PDE4A;CDC37
PDE4A;CDC37
CUI: C0011581
Disease:
Depressive disorder 		0.010 GeneticVariation BEFREE Q31L mutants had lower PDE4B activity, consistent with their resistance to rolipram, suggesting decreased PDE4 activity as a contributory factor in depression. 17481393 2007