{{Rsnum
|rsid=80338882
|Chromosome=7
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=TFR2
|position=100630973
|Gene_s=TFR2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=80338882
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=100228596
|CHROM=7
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=TFR2:7036
|GENE_NAME=TFR2
|GENE_ID=7036
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.100228596G>A
|CLNSRC=GeneReviews
|CLNORIGIN=0
|CLNSRCID=NBK1349
|CLNSIG=5
|CLNCUI=C1858664
|CLNDBN=Hemochromatosis type 3
|Disease=Hemochromatosis type 3
|CLNACC=RCV000020534.1
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1349:C1858664:604250:225123
}}{{PMID Auto
|PMID=16424658
|Title=Hemochromatosis and severe iron overload associated with compound heterozygosity for TFR2 R455Q and two novel mutations TFR2 R396X and G792R.
}}