RAD51B, RAD51 paralog B, 5890

N. diseases: 126; N. variants: 108
Disease: Primary biliary cirrhosis ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs911263
rs911263
Entrez Id: 5890
Gene Symbol: RAD51B
RAD51B
CUI: C0008312
Disease:
Primary biliary cirrhosis 		T 0.800 GeneticVariation GWASCAT International genome-wide meta-analysis identifies new primary biliary cirrhosis risk loci and targetable pathogenic pathways. 26394269 2015
dbSNP: rs911263
rs911263
Entrez Id: 5890
Gene Symbol: RAD51B
RAD51B
CUI: C0008312
Disease:
Primary biliary cirrhosis 		0.800 GeneticVariation GWASDB Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis. 22961000 2012
dbSNP: rs911263
rs911263
Entrez Id: 5890
Gene Symbol: RAD51B
RAD51B
CUI: C0008312
Disease:
Primary biliary cirrhosis 		A 0.800 GeneticVariation GWASCAT Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis. 22961000 2012
dbSNP: rs911263
rs911263
Entrez Id: 5890
Gene Symbol: RAD51B
RAD51B
CUI: C0008312
Disease:
Primary biliary cirrhosis 		T 0.800 GeneticVariation GWASDB Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. 21399635 2011
dbSNP: rs911263
rs911263
Entrez Id: 5890
Gene Symbol: RAD51B
RAD51B
CUI: C0008312
Disease:
Primary biliary cirrhosis 		T 0.800 GeneticVariation GWASCAT Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. 21399635 2011