{{Rsnum
|rsid=75030001
|Chromosome=10
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=RET
|position=43118458
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=RET
}}{{omim
|id=164761
|rsnum=75030001
|variant=0033
}}{{ClinVar
|rsid=75030001
|Reversed=0
|FwdREF=G
|FwdALT=C,T
|REF=G
|ALT=C,T
|RSPOS=43613906
|CHROM=10
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050268000000000002110100
|GENEINFO=RET:5979
|GENE_NAME=RET
|GENE_ID=5979
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000010.10:g.43613906G>C; NC_000010.10:g.43613906G>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=164761.0033
|CLNSIG=5
|CLNCUI=C0025268; C1833921
|CLNDBN=Multiple endocrine neoplasia, type 2a; Familial medullary thyroid carcinoma; MEN2A and FMTC
|Disease=Multiple endocrine neoplasia; Familial medullary thyroid carcinoma; MEN2A and FMTC
|CLNACC=RCV000014960.20; RCV000014961.20; RCV000021849.1; RCV000032038.1
|Tags=PM;PMC;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT; GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1257:C0025268:171400:247698:653:61808009; NBK1257:C1833921:155240:653
}}{{PMID Auto
|PMID=9506724
|Title=A new hot spot for mutations in the ret protooncogene causing familial medullary thyroid carcinoma and multiple endocrine neoplasia type 2A.
}}