Source: GWASCAT

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs144432435
rs144432435
CUI: C0019569
Disease: Hirschsprung Disease
Hirschsprung Disease 		T 0.710 GeneticVariation GWASCAT Genome-wide association study of Hirschsprung disease detects a novel low-frequency variant at the RET locus. 29379196

2018