{{Rsnum
|rsid=78935588
|Chromosome=10
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=RET
|position=43114519
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=RET
}}{{omim
|id=164761
|rsnum=78935588
|variant=0040
}}{{ClinVar
|rsid=78935588
|Reversed=0
|FwdREF=C
|FwdALT=G
|REF=C
|ALT=G
|RSPOS=43609967
|CHROM=10
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050068000000000002110100
|GENEINFO=RET:5979
|GENE_NAME=RET
|GENE_ID=5979
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000010.10:g.43609967C>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=164761.0040
|CLNSIG=5
|CLNCUI=C0025268
|CLNDBN=Multiple endocrine neoplasia, type 2a; MEN2 phenotype: Unknown
|Disease=Multiple endocrine neoplasia; MEN2 phenotype: Unknown
|CLNACC=RCV000014969.24; RCV000021832.1
|Tags=PM;PMC;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT; MedGen
|CLNDSDBID=NBK1257:C0025268:171400:247698:653:61808009; CN076151
}}{{PMID|10522989}} A novel case of multiple endocrine neoplasia type 2A associated with two de novo mutations of the RET protooncogene.