{{Rsnum
|rsid=2505535
|Gene=RET
|Chromosome=10
|position=43593043
|Orientation=minus
|GMAF=0.2576
|Assembly=GRCh37
|GenomeBuild=37.1
|dbSNPBuild=131
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}
{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 47.8 | 48.7 | 3.5
| HCB | 23.4 | 48.2 | 28.5
| JPT | 29.2 | 50.4 | 20.4
| YRI | 95.9 | 4.1 | 0.0
| ASW | 87.7 | 12.3 | 0.0
| CHB | 23.4 | 48.2 | 28.5
| CHD | 27.5 | 51.4 | 21.1
| GIH | 44.6 | 45.5 | 9.9
| LWK | 93.6 | 6.4 | 0.0
| MEX | 74.1 | 20.7 | 5.2
| MKK | 64.7 | 30.1 | 5.1
| TSI | 57.8 | 35.3 | 6.9
| HapMapRevision=28
}}

{{PMID|18612588}} the C allele of rs2505535 would appear to represent a protecting allele for the Chinese population

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

{{PMID Auto
|PMID=20532249
|Title=Haplotype analysis reveals a possible founder effect of RET mutation R114H for Hirschsprung's disease in the Chinese population.
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}