{{Rsnum
|rsid=77503355
|Chromosome=10
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=RET
|position=43113655
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=RET
}}{{omim
|id=164761
|rsnum=77503355
|variant=0024
}}
{{omim
|id=164761
|rsnum=77503355
|variant=0041
}}{{ClinVar
|rsid=77503355
|Reversed=0
|FwdREF=G
|FwdALT=A,C,T
|REF=G
|ALT=A,C,T
|RSPOS=43609103
|CHROM=10
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050060000000000002110104
|GENEINFO=RET:5979
|GENE_NAME=RET
|GENE_ID=5979
|WGT=0
|VC=SNV
|CLNALLE=1; 2; 3
|CLNHGVS=NC_000010.10:g.43609103G>A; NC_000010.10:g.43609103G>C; NC_000010.10:g.43609103G>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=164761.0010; 164761.0041; 164761.0024
|CLNSIG=5
|CLNCUI=C0025268; C1833921
|CLNDBN=Multiple endocrine neoplasia, type 2a; MEN2A and FMTC; Familial medullary thyroid carcinoma
|Disease=Multiple endocrine neoplasia; MEN2A and FMTC; Familial medullary thyroid carcinoma
|CLNACC=RCV000014936.24; RCV000021801.1; RCV000014970.20; RCV000021802.1; RCV000014953.20; RCV000021803.1
|Tags=PM;OTHERKG;LSD;OM;NOV
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT; GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1257:C0025268:171400:247698:653:61808009; NBK1257:C1833921:155240:653
}}