{{Rsnum
|rsid=77709286
|Chromosome=10
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=RET
|position=43114502
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=RET
}}{{omim
|id=164761
|rsnum=77709286
|variant=0012
}}{{ClinVar
|rsid=77709286
|Reversed=0
|FwdREF=C
|FwdALT=G
|REF=C
|ALT=G
|RSPOS=43609950
|CHROM=10
|dbSNPBuildID=131
|SSR=0
|SAO=3
|VP=0x050068000000000002110120
|GENEINFO=RET:5979
|GENE_NAME=RET
|GENE_ID=5979
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000010.10:g.43609950C>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=164761.0012
|CLNSIG=5
|CLNCUI=C0025268; C0031511
|CLNDBN=Multiple endocrine neoplasia, type 2a; Pheochromocytoma; MEN2A and FMTC
|Disease=Multiple endocrine neoplasia; Pheochromocytoma; MEN2A and FMTC
|CLNACC=RCV000014939.20; RCV000014940.24; RCV000021827.1
|Tags=PM;PMC;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT; GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1257:C0025268:171400:247698:653:61808009; NBK1548:C0031511:171300:29072
}}{{PMID Auto
|PMID=7907913
|Title=Specific mutations of the RET proto-oncogene are related to disease phenotype in MEN 2A and FMTC.
}}

{{PMID Auto
|PMID=12000816
|Title=Germ-line mutations in nonsyndromic pheochromocytoma.
}}