{{Rsnum
|rsid=3026785
|Gene=RET
|Chromosome=10
|position=43130238
|Orientation=plus
|GMAF=0.03398
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=RET
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 0.0 | 10.5 | 89.5
| HCB | 0.0 | 0.0 | 100.0
| JPT | 0.0 | 6.2 | 93.8
| YRI | 0.0 | 6.2 | 93.8
| ASW | 0.0 | 3.5 | 96.5
| CHB | 0.0 | 0.0 | 100.0
| CHD | 0.0 | 2.9 | 97.1
| GIH | 0.0 | 24.8 | 75.2
| LWK | 0.0 | 7.4 | 92.6
| MEX | 1.8 | 7.1 | 91.1
| MKK | 0.6 | 7.1 | 92.3
| TSI | 0.0 | 14.0 | 86.0
| HapMapRevision=28
}}Associated with protection from [[Hirschsprung disease]]

See OMIM [http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=164761&a=164761_AllelicVariant0052 164761.0052]

{{omim
|id=164761
|rsnum=3026785
|variant=0052
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}