{{Rsnum
|rsid=1800861
|Gene=RET
|Chromosome=10
|position=43118395
|Orientation=minus
|GMAF=0.2773
|Gene_s=RET
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{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=A,T
|CAF=0.2773; 0.7227
|CHROM=10
|CLNACC=RCV000021844.1
|CLNALLE=0
|CLNDBN=No MEN2 disease
|CLNHGVS=NC_000010.10:g.43613843G\x3d
|CLNSIG=2
|COMMON=1
|Disease=No MEN2 disease
|FwdALT=A,T
|FwdREF=C
|GENEINFO=RET:5979
|GENE_ID=5979
|GENE_NAME=RET
|REF=G
|RSPOS=43613843
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;S3D;SLO;VLD;G5A;G5;HD;GNO;KGPhase1;KGPilot123;KGPROD;OTHERKG;LSD
|VC=SNV
|VP=0x05036800000017051e100100
|WGT=0
|dbSNPBuildID=89
|rsid=1800861
}}

{{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=19379518
|Title=Development of a fingerprinting panel using medically relevant polymorphisms.
|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=20565774
|Title=Population based allele frequencies of disease associated polymorphisms in the Personalized Medicine Research Project.
|OA=1
}}

{{PMID Auto
|PMID=21349203
|Title=Genetic variants in RET and risk of Hirschsprung's disease in Southeastern Chinese: a haplotype-based analysis.
|OA=1
}}

{{PMID Auto
|PMID=8084609
|Title=DNA polymorphisms and conditions for SSCP analysis of the 20 exons of the ret proto-oncogene.
}}

{{PMID Auto
|PMID=24897126
|Title=RET Variants and Haplotype Analysis in a Cohort of Czech Patients with Hirschsprung Disease
}}
{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}