{{Rsnum
|rsid=80236571
|Chromosome=10
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=RET
|position=43106497
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=LOC100288973,RET
}}{{omim
|id=164761
|rsnum=80236571
|variant=0022
}}{{ClinVar
|rsid=80236571
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=43601945
|CHROM=10
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=RET:5979
|GENE_NAME=RET
|GENE_ID=5979
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000010.10:g.43601945G>A
|CLNORIGIN=0
|CLNSIG=255
|Tags=PM;OTHERKG;LSD;OM
|CLNACC=RCV000014951.1
|CLNDBN=Hirschsprung disease 1
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1439:CN030431:142623:388:204739008
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=164761.0022
|Disease=Hirschsprung disease 1
}}