{{Rsnum
|rsid=77939446
|Chromosome=10
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=RET
|position=43113622
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=RET
}}{{omim
|id=164761
|rsnum=77939446
|variant=0029
}}{{ClinVar
|rsid=77939446
|Reversed=0
|FwdREF=G
|FwdALT=A,C,T
|REF=G
|ALT=A,C,T
|RSPOS=43609070
|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.43609070G>A; NC_000010.10:g.43609070G>C; NC_000010.10:g.43609070G>T
|CLNORIGIN=0
|CLNSIG=5
|Tags=PM;PMC;OTHERKG;LSD;OM;NOV
|CLNACC=RCV000014958.24; RCV000021778.1; RCV000082049.1; RCV000021779.1; RCV000021780.1
|CLNDBN=MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA, WITH HIRSCHSPRUNG DISEASE; MEN2A and FMTC; not provided; Multiple endocrine neoplasia, type 2a; MEN2A and Unclassified
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1257:C0025268:171400:247698:653:61808009
|CLNSRC=Emory University; OMIM Allelic Variant
|CLNSRCID=6625; 164761.0029
|Disease=MULTIPLE ENDOCRINE NEOPLASIA; MEN2A and FMTC; not provided; Multiple endocrine neoplasia; MEN2A and Unclassified
}}{{PMID Auto
|PMID=11524247
|Title=Molecular genetic diagnostic program of multiple endocrine neoplasia type 2A and familial medullary thyroid carcinoma syndromes in Hungary.
}}

{{PMID Auto
|PMID=9068588
|Title=Rapid, nonradioactive screening for mutations in exons 10, 11, and 16 of the RET protooncogene associated with inherited medullary thyroid carcinoma.
}}