{{Rsnum
|rsid=78347871
|Chromosome=10
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=RET
|position=43121950
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=RET
}}{{omim
|id=164761
|rsnum=78347871
|variant=0051
}}{{ClinVar
|rsid=78347871
|Reversed=0
|FwdREF=G
|FwdALT=A,C,T
|REF=G
|ALT=A,C,T
|RSPOS=43617398
|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
|CLNHGVS=NC_000010.10:g.43617398G>A; NC_000010.10:g.43617398G>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=164761.0051
|CLNSIG=5
|CLNCUI=C1833921
|CLNDBN=MEN2 phenotype: Unknown; Familial medullary thyroid carcinoma; MEN2 phenotype: Unclassified
|Disease=MEN2 phenotype: Unknown; Familial medullary thyroid carcinoma; MEN2 phenotype: Unclassified
|CLNACC=RCV000021882.1; RCV000014981.20; RCV000021883.1
|Tags=PM;PMC;S3D;OTHERKG;LSD;OM;NOV
|CLNDSDB=MedGen; GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=CN076151; NBK1257:C1833921:155240:653; CN076152
}}{{PMID Auto
|PMID=15240641
|Title=A novel point mutation of the RET protooncogene involving the second intracellular tyrosine kinase domain in a family with medullary thyroid carcinoma.
}}{{PMID Auto
|PMID=11955539
|Title=Association between c135G/A genotype and RET proto-oncogene germline mutations and phenotype of Hirschsprung's disease.
}}