{{Rsnum
|rsid=80338877
|Chromosome=7
|Orientation=minus
|geno1=(-;-)
|geno2=(-;C)
|geno3=(C;C)
|Gene=TFR2
|position=100641173
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TFR2
}}{{omim
|id=604720
|rsnum=80338877
|variant=0002
}}{{ClinVar
|rsid=80338877
|Reversed=1
|FwdREF=CGG
|FwdALT=C
|REF=C
|ALT=CG
|RSPOS=100238796
|CHROM=7
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050168000000000002110200
|GENEINFO=TFR2:7036
|GENE_NAME=TFR2
|GENE_ID=7036
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.100238796_100238797insG
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK1349; 604720.0002
|CLNSIG=5
|CLNCUI=C1858664; C1858664
|CLNDBN=Hemochromatosis type 3
|Disease=Hemochromatosis type 3
|CLNACC=RCV000005712.1
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1349:C1858664:604250:225123
}}{{PMID Auto
|PMID=11313241
|Title=New mutations inactivating transferrin receptor 2 in hemochromatosis type 3.
}}