{{Rsnum
|rsid = 17857727
|Status = Merged
|Merged = 1800858
|Orientation=plus
|ReferenceAllele=G
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Chromosome=10
|position=43100520
|Gene=RET
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=RET
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 3.5 | 48.7 | 47.8
| HCB | 28.7 | 48.5 | 22.8
| JPT | 20.4 | 49.6 | 30.1
| YRI | 0.0 | 4.1 | 95.9
| ASW | 0.0 | 12.3 | 87.7
| CHB | 28.7 | 48.5 | 22.8
| CHD | 21.1 | 51.4 | 27.5
| GIH | 9.9 | 45.5 | 44.6
| LWK | 0.0 | 7.3 | 92.7
| MEX | 5.2 | 20.7 | 74.1
| MKK | 5.1 | 30.8 | 64.1
| TSI | 6.9 | 33.7 | 59.4
| HapMapRevision=28
}}
{{omim
| id = 164761
| variant = 0038
| desc    = HIRSCHSPRUNG DISEASE
| rsnum   = 17857727
}}
{{ neighbor
| rsid = 1800858
| distance = 1
}}