rs117617821, None

N. diseases: 2
Disease: Congenital Intestinal Aganglionosis ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Congenital Intestinal Aganglionosis
CUI: C3661523
Disease: Congenital Intestinal Aganglionosis
0.700 GeneticVariation GWASCAT Genome-wide association study of Hirschsprung disease detects a novel low-frequency variant at the RET locus. 29379196 2018