{{Rsnum
|rsid=77724903
|Chromosome=10
|Orientation=plus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=RET
|position=43118460
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=RET
}}{{omim
|id=164761
|rsnum=77724903
|variant=0034
}}{{ClinVar
|rsid=77724903
|Reversed=0
|FwdREF=A
|FwdALT=T
|REF=A
|ALT=T
|RSPOS=43613908
|CHROM=10
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050268000000040002110100
|GENEINFO=RET:5979
|GENE_NAME=RET
|GENE_ID=5979
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000010.10:g.43613908A>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=164761.0034
|CLNSIG=5
|CLNCUI=C1833921; C0031511
|CLNDBN=Familial medullary thyroid carcinoma; Pheochromocytoma; MEN2A and FMTC; not provided
|Disease=Familial medullary thyroid carcinoma; Pheochromocytoma; MEN2A and FMTC; not provided
|CLNACC=RCV000014962.24; RCV000014963.24; RCV000021851.1; RCV000034771.1
|Tags=PM;PMC;S3D;VLD;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1257:C1833921:155240:653; NBK1548:C0031511:171300:29072
}}{{PMID Auto
|PMID=12000816
|Title=Germ-line mutations in nonsyndromic pheochromocytoma.
}}

{{PMID Auto
|PMID=16118333
|Title=Polymorphisms in exon 13 and intron 14 of the RET protooncogene: genetic modifiers of medullary thyroid carcinoma?
}}