Gene: RET ×
Source: GWASCAT ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2435357
rs2435357
RET
0.900 GeneticVariation GWASCAT Excluding the rare variant carriers from the genome-wide association analysis did not appreciably change the association of rs2435357 with Hirschsprung disease. 30031151

2019
dbSNP: rs2742234
rs2742234
RET
T 0.800 GeneticVariation GWASCAT Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease. 19196962

2009
dbSNP: rs9282834
rs9282834
RET
A 0.710 GeneticVariation GWASCAT Trans-ethnic meta-analysis of genome-wide association studies for Hirschsprung disease. 27702942

2016
dbSNP: rs2505998
rs2505998
RET
A 0.700 GeneticVariation GWASCAT Trans-ethnic meta-analysis of genome-wide association studies for Hirschsprung disease. 27702942

2016
dbSNP: rs1864400
rs1864400
RET
0.700 GeneticVariation GWASCAT A genome-wide association study identifies potential susceptibility loci for Hirschsprung disease. 25310821

2014