{{Rsnum
|rsid=77558292
|Chromosome=10
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=RET
|position=43113621
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=RET
}}{{omim
|id=164761
|rsnum=77558292
|variant=0042
}}{{ClinVar
|rsid=77558292
|Reversed=0
|FwdREF=T
|FwdALT=A,C,G
|REF=T
|ALT=A,C,G
|RSPOS=43609069
|CHROM=10
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050068000000000002110104
|GENEINFO=RET:5979
|GENE_NAME=RET
|GENE_ID=5979
|WGT=0
|VC=SNV
|CLNALLE=1; 2; 3
|CLNHGVS=NC_000010.10:g.43609069T>A; NC_000010.10:g.43609069T>C; NC_000010.10:g.43609069T>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=164761.0042
|CLNSIG=5
|CLNCUI=C1833921
|CLNDBN=MEN2 phenotype: Unknown; Familial medullary thyroid carcinoma; MEN2A and FMTC; Multiple endocrine neoplasia, type 2a
|Disease=MEN2 phenotype: Unknown; Familial medullary thyroid carcinoma; MEN2A and FMTC; Multiple endocrine neoplasia
|CLNACC=RCV000021775.1; RCV000014971.24; RCV000021776.1; RCV000021777.1
|Tags=PM;PMC;OTHERKG;LSD;OM;NOV
|CLNDSDB=MedGen; GeneReviews:MedGen:OMIM:Orphanet; GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=CN076151; NBK1257:C1833921:155240:653; NBK1257:C0025268:171400:247698:653:61808009
}}{{PMID Auto
|PMID=10982477
|Title=Familial form of hirschsprung disease: nucleotide sequence studies reveal point mutations in the RET proto-oncogene in two of six families but not in other candidate genes.
}}{{PMID Auto
|PMID=11955539
|Title=Association between c135G/A genotype and RET proto-oncogene germline mutations and phenotype of Hirschsprung's disease.
}}

{{PMID Auto
|PMID=8626834
|Title=Mutations of the ret protooncogene in German multiple endocrine neoplasia families: relation between genotype and phenotype. German Medullary Thyroid Carcinoma Study Group.
}}