{{Rsnum
|rsid=1800862
|Gene=RET
|Chromosome=10
|position=43119646
|Orientation=plus
|GMAF=0.03168
|Gene_s=RET
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{PMID Auto
|PMID=23059849
|Title=Medullary thyroid carcinoma (MTC) and RET proto-oncogene: mutation spectrum in the familial cases and a meta-analysis of studies on the sporadic form
}}

{{ClinVar
|ALT=T
|CAF=0.9683; 0.03168
|CHROM=10
|CLNACC=RCV000021860.1
|CLNALLE=1
|CLNDBN=No MEN2 disease
|CLNHGVS=NC_000010.10:g.43615094C>T
|CLNSIG=2
|COMMON=1
|Disease=No MEN2 disease
|FwdALT=T
|FwdREF=C
|GENEINFO=RET:5979
|GENE_ID=5979
|GENE_NAME=RET
|REF=C
|RSPOS=43615094
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;S3D;SLO;VLD;G5;GNO;KGPhase1;KGPROD;OTHERKG;LSD
|VC=SNV
|VP=0x050368000000150116100100
|WGT=0
|dbSNPBuildID=89
|rsid=1800862
}}

{{PMID Auto
|PMID=19138047
|Title=Thyroid nodules, polymorphic variants in DNA repair and RET-related genes, and interaction with ionizing radiation exposure from nuclear tests in Kazakhstan.
|OA=1
}}

{{PMID Auto
|PMID=20532249
|Title=Haplotype analysis reveals a possible founder effect of RET mutation R114H for Hirschsprung's disease in the Chinese population.
|OA=1
}}

{{PMID Auto
|PMID=10022819
|Title=Over-representation of a germline RET sequence variant in patients with sporadic medullary thyroid carcinoma and somatic RET codon 918 mutation.
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}