STH, saitohin, 246744

N. diseases: 1; N. variants: 4
Source: CURATED ×
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs62063857
rs62063857
Entrez Id: 4137;246744
Gene Symbol: MAPT;STH
MAPT;STH
CUI: C0008312
Disease:
Primary biliary cirrhosis
0.700 GeneticVariation GWASDB Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis. 22961000 2012