{{Rsnum
|rsid=193922699
|Chromosome=10
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=RET
|position=43114478
|Gene_s=RET
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=193922699
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=43609926
|CHROM=10
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050068000000000002100100
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000010.10:g.43609926A>G
|CLNSRC=Correlagen
|CLNORIGIN=1
|CLNSIG=4
|CLNDBN=Hirschsprung disease 1
|Disease=Hirschsprung disease 1
|Tags=PM;PMC;OTHERKG;LSD
|CLNACC=RCV000030404.1
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1439:CN030431:142623:388:204739008
|GENEINFO=RET:5979
|GENE_ID=5979
|GENE_NAME=RET
}}{{PMID Auto
|PMID=11436122
|Title=Novel RET mutations in Hirschsprung's disease patients from the diverse South African population.
}}

{{PMID Auto
|PMID=12628594
|Title=Significance of novel endothelin-B receptor gene polymorphisms in Hirschsprung's disease: predominance of a novel variant (561C/T) in patients with co-existing Down's syndrome.
}}

{{PMID Auto
|PMID=18280283
|Title=A review of genetic mutation in familial Hirschsprung's disease in South Africa: towards genetic counseling.
}}

{{PMID Auto
|PMID=19572138
|Title=Total colonic aganglionosis and Hirschsprung's disease: shades of the same or different?
}}

{{PMID Auto
|PMID=19853744
|Title=Clinical and genetic differences in total colonic aganglionosis in Hirschsprung's disease.
}}