{{Rsnum
|rsid=2506004
|Gene=RET
|Chromosome=10
|position=43582273
|Orientation=minus
|GMAF=0.2599
|Gene_s=RET
|Assembly=GRCh37.p5
|GenomeBuild=37.3
|dbSNPBuild=135
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}
{{PMID Auto
|PMID=22325379
|Title=Intronic RET gene variants in Down syndrome-associated Hirschsprung disease in an African population
}}

{{PMID|15759212|OA=1
}} Identifying candidate Hirschsprung disease-associated RET variants.

{{PMID|20977903}} Variants in RET associated with Hirschsprung's disease affect binding of transcription factors and gene expression.

{{PMID Auto
|PMID=24897126
|Title=RET Variants and Haplotype Analysis in a Cohort of Czech Patients with Hirschsprung Disease
}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}