{{Rsnum
|rsid=75234356
|Chromosome=10
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=RET
|position=43120144
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=RET
}}{{omim
|id=164761
|rsnum=75234356
|variant=0049
}}{{ClinVar
|rsid=75234356
|Reversed=0
|FwdREF=T
|FwdALT=G
|REF=T
|ALT=G
|RSPOS=43615592
|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
|CLNHGVS=NC_000010.10:g.43615592T>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=164761.0049
|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=RCV000014978.24; RCV000014979.24; RCV000021875.1
|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=10024437
|Title=A codon 891 exon 15 RET proto-oncogene mutation in familial medullary thyroid carcinoma: a detection strategy.
}}