Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs199515
rs199515
Entrez Id: 7473;474170
Gene Symbol: WNT3;LRRC37A2
WNT3;LRRC37A2
CUI: C0008312
Disease:
Primary biliary cirrhosis
0.700 GeneticVariation GWASDB Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis. 22961000 2012