{{Rsnum
|rsid=79890926
|Chromosome=10
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=RET
|position=43113656
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=RET
}}{{omim
|id=164761
|rsnum=79890926
|variant=0032
}}{{ClinVar
|rsid=79890926
|Reversed=0
|FwdREF=C
|FwdALT=G
|REF=C
|ALT=G
|RSPOS=43609104
|CHROM=10
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=RET:5979
|GENE_NAME=RET
|GENE_ID=5979
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000010.10:g.43609104C>G
|CLNORIGIN=0
|CLNSIG=5
|Tags=PM;OTHERKG;LSD;OM
|CLNACC=RCV000014959.24; RCV000021789.1
|CLNDBN=MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA, WITH HIRSCHSPRUNG DISEASE; MEN2A and Unclassified
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=164761.0032
|Disease=MULTIPLE ENDOCRINE NEOPLASIA; MEN2A and Unclassified
}}