{{Rsnum
|rsid=75873440
|Chromosome=10
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=RET
|position=43112173
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=RET
}}{{omim
|id=164761
|rsnum=75873440
|variant=0048
}}{{ClinVar
|rsid=75873440
|Reversed=0
|FwdREF=G
|FwdALT=A,T
|REF=G
|ALT=A,T
|RSPOS=43607621
|CHROM=10
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050068000000000002110100
|GENEINFO=RET:5979
|GENE_NAME=RET
|GENE_ID=5979
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000010.10:g.43607621G>A; NC_000010.10:g.43607621G>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=164761.0048
|CLNSIG=5
|CLNCUI=C1833921
|CLNDBN=MEN2 phenotype: Unknown; Familial medullary thyroid carcinoma; MEN2A and FMTC
|Disease=MEN2 phenotype: Unknown; Familial medullary thyroid carcinoma; MEN2A and FMTC
|CLNACC=RCV000021768.1; RCV000014977.20; RCV000021770.1
|Tags=PM;PMC;OTHERKG;LSD;OM
|CLNDSDB=MedGen; GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=CN076151; NBK1257:C1833921:155240:653
}}{{PMID Auto
|PMID=14602786
|Title=A novel germ-line point mutation in RET exon 8 (Gly(533)Cys) in a large kindred with familial medullary thyroid carcinoma.
}}{{PMID Auto
|PMID=17009072
|Title=Mutations and polymorphisms of Hirschsprung disease candidate genes in Thai patients.
}}