{{Rsnum
|rsid=80338885
|Chromosome=7
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=TFR2
|position=100628294
|Gene_s=TFR2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=80338885
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=100225917
|CHROM=7
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050368000000040002110100
|GENEINFO=TFR2:7036
|GENE_NAME=TFR2
|GENE_ID=7036
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.100225917C>T
|CLNSRC=GeneReviews
|CLNORIGIN=0
|CLNSRCID=NBK1349
|CLNSIG=5
|CLNCUI=C1858664
|CLNDBN=Hemochromatosis type 3
|Disease=Hemochromatosis type 3
|CLNACC=RCV000020538.1
|Tags=RV;PM;PMC;S3D;SLO;VLD;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1349:C1858664:604250:225123
}}{{PMID|17562347}} A novel mutation of transferrin receptor 2 in a Taiwanese woman with type 3 hemochromatosis.