{{Rsnum
|rsid=80338888
|Chromosome=7
|Orientation=minus
|geno1=(-;-)
|geno2=(-;GCCGTGGCCCAG)
|geno3=(GCCGTGGCCCAG;GCCGTGGCCCAG)
|Gene=TFR2
|position=100627387
|Gene_s=TFR2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=7
|CLNACC=RCV000020543.1
|CLNALLE=1
|CLNDBN=Hemochromatosis type 3
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1349:C1858664:604250:225123
|CLNHGVS=NC_000007.13:g.100225010_100225021delCTGGGCCACGGC
|CLNORIGIN=0
|CLNSIG=5
|CLNSRC=GeneReviews
|CLNSRCID=NBK1349
|Disease=Hemochromatosis type 3
|FwdREF=GCCGTGGCCCAG
|GENEINFO=TFR2:7036
|GENE_ID=7036
|GENE_NAME=TFR2
|REF=GCTGGGCCACGGC
|RSPOS=100225009
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050168000000000002110200
|WGT=0
|dbSNPBuildID=131
|rsid=80338888
}}{{PMID Auto
|PMID=11984516
|Title=Clinical and pathologic findings in hemochromatosis type 3 due to a novel mutation in transferrin receptor 2 gene.
}}