rs1864400, RET

N. diseases: 2
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Hirschsprung Disease
CUI: C0019569
Disease: Hirschsprung Disease
0.700 GeneticVariation GWASCAT A genome-wide association study identifies potential susceptibility loci for Hirschsprung disease. 25310821 2014
Congenital Intestinal Aganglionosis
CUI: C3661523
Disease: Congenital Intestinal Aganglionosis
0.700 GeneticVariation GWASCAT A genome-wide association study identifies potential susceptibility loci for Hirschsprung disease. 25310821 2014