Disease: Digestive System Disorders ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10419226
rs10419226
Entrez Id: 23373
Gene Symbol: CRTC1
CRTC1
CUI: C0012242
Disease:
Digestive System Disorders 		A 0.700 GeneticVariation GWASCAT A genome-wide association study identifies new susceptibility loci for esophageal adenocarcinoma and Barrett's esophagus. 24121790 2013