rs2742234, 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
0.800 GeneticVariation GWASCAT Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease. 19196962 2009
Hirschsprung Disease
CUI: C0019569
Disease: Hirschsprung Disease
0.800 GeneticVariation GWASDB Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease. 19196962 2009
Congenital Intestinal Aganglionosis
CUI: C3661523
Disease: Congenital Intestinal Aganglionosis
0.700 GeneticVariation GWASCAT Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease. 19196962 2009