{{Rsnum
|rsid=79658334
|Chromosome=10
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=RET
|position=43119548
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=RET
}}{{omim
|id=164761
|rsnum=79658334
|variant=0043
}}{{ClinVar
|rsid=79658334
|Reversed=0
|FwdREF=G
|FwdALT=A,C,T
|REF=G
|ALT=A,C,T
|RSPOS=43614996
|CHROM=10
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050268000000000002110104
|GENEINFO=RET:5979
|GENE_NAME=RET
|GENE_ID=5979
|WGT=0
|VC=SNV
|CLNALLE=1; 2; 3
|CLNHGVS=NC_000010.10:g.43614996G>A; NC_000010.10:g.43614996G>C; NC_000010.10:g.43614996G>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=0; 1
|CLNSRCID=164761.0043; 164761.0044
|CLNSIG=5
|CLNCUI=C1833921
|CLNDBN=Multiple endocrine neoplasia, type 2b; MEN2A and FMTC; MEN2 phenotype: Unclassified; Familial medullary thyroid carcinoma
|Disease=Multiple endocrine neoplasia; MEN2A and FMTC; MEN2 phenotype: Unclassified; Familial medullary thyroid carcinoma
|CLNACC=RCV000014972.24; RCV000021852.1; RCV000021853.1; RCV000014973.24; RCV000021854.1
|Tags=PM;PMC;S3D;OTHERKG;LSD;OM;NOV
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT:SNOMED_CT; MedGen; GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1257:C0025269:162300:653:6153000:61530001; CN076152; NBK1257:C1833921:155240:653
}}{{PMID Auto
|PMID=11589684
|Title=Germline sequence variant S836S in the RET proto-oncogene is associated with low level predisposition to sporadic medullary thyroid carcinoma in the Spanish population.
}}

{{PMID Auto
|PMID=12694233
|Title=Segregation of the V804L mutation and S836S polymorphism of exon 14 of the RET gene in an extended kindred with familial medullary thyroid cancer.
}}

{{PMID Auto
|PMID=15741265
|Title=Germline homozygous mutations at codon 804 in the RET protooncogene in medullary thyroid carcinoma/multiple endocrine neoplasia type 2A patients.
}}