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

2018
dbSNP: rs144432435
rs144432435 		0.710 GeneticVariation BEFREE The conditional signal was, however, not replicated in two HSCR cohorts from USA and Finland, leading to the hypothesis that rs144432435 tags a rare haplotype present in Denmark and Sweden. 29379196

2018