{{Rsnum
|rsid=80338880
|Chromosome=7
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=TFR2
|position=100633100
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TFR2
}}{{omim
|id=604720
|rsnum=80338880
|variant=0001
}}{{ClinVar
|rsid=80338880
|Reversed=1
|FwdREF=C
|FwdALT=G
|REF=G
|ALT=C
|RSPOS=100230723
|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.100230723G>C
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1349; 604720.0001
|CLNSIG=5
|CLNCUI=C1858664; C1858664
|CLNDBN=Hemochromatosis type 3
|Disease=Hemochromatosis type 3
|CLNACC=RCV000005711.1
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1349:C1858664:604250:225123
}}{{PMID Auto
|PMID=10802645
|Title=The gene TFR2 is mutated in a new type of haemochromatosis mapping to 7q22.
}}