{{Rsnum
|rsid=2472737
|Gene=RET
|Chromosome=10
|position=43120057
|Orientation=plus
|GMAF=0.1873
|Gene_s=RET
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 6.2 | 34.5 | 59.3
| HCB | 3.6 | 32.1 | 64.2
| JPT | 1.8 | 26.5 | 71.7
| YRI | 0.7 | 23.1 | 76.2
| ASW | 0.0 | 21.1 | 78.9
| CHB | 3.6 | 32.1 | 64.2
| CHD | 4.6 | 33.0 | 62.4
| GIH | 2.0 | 21.8 | 76.2
| LWK | 1.8 | 22.7 | 75.5
| MEX | 1.7 | 27.6 | 70.7
| MKK | 1.3 | 26.9 | 71.8
| TSI | 2.9 | 39.2 | 57.8
| HapMapRevision=28
}}{{PMID Auto
|PMID=16118333
|Title=Polymorphisms in exon 13 and intron 14 of the RET protooncogene: genetic modifiers of medullary thyroid carcinoma?
}}

{{ClinVar
|ALT=A
|CAF=0.8127; 0.1873
|CHROM=10
|CLNACC=RCV000021870.1; RCV000082053.1
|CLNALLE=1
|CLNDBN=No MEN2 disease; AllHighlyPenetrant
|CLNHGVS=NC_000010.10:g.43615505G>A
|CLNSIG=2
|COMMON=1
|Disease=No MEN2 disease; AllHighlyPenetrant
|FwdALT=A
|FwdREF=G
|GENEINFO=RET:5979
|GENE_ID=5979
|GENE_NAME=RET
|REF=G
|RSPOS=43615505
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;SLO;VLD;G5A;G5;HD;GNO;KGPhase1;KGPilot123;KGPROD;OTHERKG;PH3;LSD
|VC=SNV
|VP=0x05016800000007051f100101
|WGT=0
|dbSNPBuildID=100
|rsid=2472737
|CLNDSDB=MedGen
|CLNDSDBID=CN169374
}}

{{PMID Auto
|PMID=11302967
|Title=Analysis of the RET, GDNF, EDN3, and EDNRB genes in patients with intestinal neuronal dysplasia and Hirschsprung disease.
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | Illumina Human 1M}}