CNTN5, contactin 5, 53942

N. diseases: 34; N. variants: 20
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: rs1939707
rs1939707
Entrez Id: 53942
Gene Symbol: CNTN5
CNTN5
CUI: C0008312
Disease:
Primary biliary cirrhosis 		0.700 GeneticVariation GWASDB Genome-wide association study identifies TNFSF15 and POU2AF1 as susceptibility loci for primary biliary cirrhosis in the Japanese population. 23000144 2012