{{Rsnum
|rsid=78014899
|Chromosome=10
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=RET
|position=43118392
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=RET
}}{{omim
|id=164761
|rsnum=78014899
|variant=0027
}}{{ClinVar
|rsid=78014899
|Reversed=0
|FwdREF=G
|FwdALT=A,C,T
|REF=G
|ALT=A,C,T
|RSPOS=43613840
|CHROM=10
|dbSNPBuildID=131
|SSR=0
|SAO=3
|VP=0x050268000000000002110124
|GENEINFO=RET:5979
|GENE_NAME=RET
|GENE_ID=5979
|WGT=0
|VC=SNV
|CLNALLE=2; 3
|CLNHGVS=NC_000010.10:g.43613840G>C; NC_000010.10:g.43613840G>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=2
|CLNSRCID=164761.0027
|CLNSIG=5
|CLNCUI=C1833921
|CLNDBN=Familial medullary thyroid carcinoma; MEN2A and FMTC; MEN2 phenotype: Unclassified
|Disease=Familial medullary thyroid carcinoma; MEN2A and FMTC; MEN2 phenotype: Unclassified
|CLNACC=RCV000014956.24; RCV000021842.1; RCV000032037.1
|Tags=PM;PMC;S3D;OTHERKG;LSD;OM;NOV
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; MedGen
|CLNDSDBID=NBK1257:C1833921:155240:653; CN076152
}}{{PMID Auto
|PMID=9111992
|Title=Mutation of RET codon 768 is associated with the FMTC phenotype.
}}

{{PMID Auto
|PMID=12116277
|Title=A novel germline point mutation, c.2304 G-->T, in codon 768 of the RET proto-oncogene in a patient with medullary thyroid carcinoma.
}}{{PMID Auto
|PMID=11230481
|Title=Estimation of risk of inherited medullary thyroid carcinoma in apparent sporadic patients.
}}