{{Rsnum
|rsid=76764689
|Chromosome=10
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=RET
|position=43100480
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=RET
}}{{omim
|id=164761
|rsnum=76764689
|variant=0018
}}{{ClinVar
|rsid=76764689
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=43595928
|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.43595928C>T
|CLNORIGIN=1
|CLNSIG=255
|Tags=PM;OTHERKG;LSD;OM
|CLNACC=RCV000014948.1
|CLNDBN=Hirschsprung disease 1
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1439:CN030431:142623:388:204739008
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=164761.0018
|Disease=Hirschsprung disease 1
}}