{{Rsnum
|rsid=41303501
|Gene=TFR2
|Chromosome=7
|position=100629279
|Orientation=plus
|GMAF=0.001377
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=TFR2
}}{{omim
|id=604720
|rsnum=41303501
|variant=0004
}}

{{ClinVar
|rsid=41303501
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=100226902
|CHROM=7
|GMAF=0.0014
|dbSNPBuildID=127
|SSR=0
|SAO=1
|VP=0x050368000000040516110100
|GENEINFO=TFR2:7036
|GENE_NAME=TFR2
|GENE_ID=7036
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.100226902C>T
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK1349; 604720.0004
|CLNSIG=5
|CLNCUI=C1858664
|CLNDBN=Hemochromatosis, type 1, modifier of; Hemochromatosis type 3
|Disease=Hemochromatosis; Hemochromatosis type 3
|CLNACC=RCV000005714.1; RCV000020537.1
|Tags=RV;PM;PMC;S3D;SLO;VLD;HD;GNO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9986; 0.001377
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1349:C1858664:604250:225123
|COMMON=0
}}

{{PMID Auto
|PMID=12150153
|Title=Mutation analysis of transferrin-receptor 2 in patients with atypical hemochromatosis.
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}