{{Rsnum
|rsid=1800858
|Gene=RET
|Chromosome=10
|position=43100520
|Orientation=plus
|ReferenceAllele=G
|GMAF=0.2842
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|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
|desc=HIRSCHSPRUNG DISEASE
|id=164761
|rsnum=1800858
|variant=0038
}}

{{ neighbor
| rsid = 17857727
| distance = 1
}}

{{PMID Auto
|PMID=20454948
|Title=Association analysis of the RET proto-oncogene with Hirschsprung disease in the Han Chinese population of southeastern China
}}

{{ClinVar
|rsid=1800858
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=43595968
|CHROM=10
|GMAF=0.2834
|dbSNPBuildID=89
|SSR=0
|SAO=1
|VP=0x05016800000015051f110100
|WGT=0
|VC=SNV
|CLNALLE=0
|CLNHGVS=NC_000010.10:g.43595968A\x3d
|CLNORIGIN=0
|CLNSIG=255
|Tags=PM;PMC;SLO;VLD;G5;HD;GNO;KGPhase1;KGPilot123;KGPROD;OTHERKG;PH3;LSD;OM
|CAF=0.2842; 0.7158
|CLNACC=RCV000014967.1
|CLNDBN=Hirschsprung disease 1
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1439:CN030431:142623:388:204739008
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=164761.0038
|COMMON=1
|Disease=Hirschsprung disease 1
|GENEINFO=RET:5979
|GENE_ID=5979
|GENE_NAME=RET
}}

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

{{PMID Auto
|PMID=17267408
|Title=Allelic imbalance in gene expression as a guide to cis-acting regulatory single nucleotide polymorphisms in cancer cells.
|OA=1
}}

{{PMID Auto
|PMID=18091754
|Title=Regional association-based fine-mapping for sodium-lithium countertransport on chromosome 10.
|OA=1
}}

{{PMID Auto
|PMID=19138047
|Title=Thyroid nodules, polymorphic variants in DNA repair and RET-related genes, and interaction with ionizing radiation exposure from nuclear tests in Kazakhstan.
|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
}}

{{PMID Auto
|PMID=21349203
|Title=Genetic variants in RET and risk of Hirschsprung's disease in Southeastern Chinese: a haplotype-based analysis.
|OA=1
}}

{{PMID Auto
|PMID=10521317
|Title=Association of RET protooncogene codon 45 polymorphism with Hirschsprung disease.
|OA=1
}}

{{PMID Auto
|PMID=10922382
|Title=RET genotypes comprising specific haplotypes of polymorphic variants predispose to isolated Hirschsprung disease.
|OA=1
}}

{{PMID Auto
|PMID=23059849
|Title=Medullary thyroid carcinoma (MTC) and RET proto-oncogene: mutation spectrum in the familial cases and a meta-analysis of studies on the sporadic form
}}

{{PMID Auto
|PMID=24897126
|Title=RET Variants and Haplotype Analysis in a Cohort of Czech Patients with Hirschsprung Disease
}}
{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}