TNFRSF1A, TNF receptor superfamily member 1A, 7132

N. diseases: 487; N. variants: 48
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: rs1800693
rs1800693
Entrez Id: 7132
Gene Symbol: TNFRSF1A
TNFRSF1A
CUI: C0008312
Disease:
Primary biliary cirrhosis 		C 0.800 GeneticVariation GWASCAT International genome-wide meta-analysis identifies new primary biliary cirrhosis risk loci and targetable pathogenic pathways. 26394269 2015
dbSNP: rs1800693
rs1800693
Entrez Id: 7132
Gene Symbol: TNFRSF1A
TNFRSF1A
CUI: C0008312
Disease:
Primary biliary cirrhosis 		G 0.800 GeneticVariation GWASCAT Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis. 22961000 2012
dbSNP: rs1800693
rs1800693
Entrez Id: 7132
Gene Symbol: TNFRSF1A
TNFRSF1A
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: rs1800693
rs1800693
Entrez Id: 7132
Gene Symbol: TNFRSF1A
TNFRSF1A
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: rs1800693
rs1800693
Entrez Id: 7132
Gene Symbol: TNFRSF1A
TNFRSF1A
CUI: C0008312
Disease:
Primary biliary cirrhosis 		C 0.800 GeneticVariation GWASCAT Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. 21399635 2011
dbSNP: rs1800693
rs1800693
Entrez Id: 7132
Gene Symbol: TNFRSF1A
TNFRSF1A
CUI: C0008312
Disease:
Primary biliary cirrhosis 		C 0.800 GeneticVariation GWASDB Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. 21399635 2011