{{Rsnum
|rsid=2075674
|Gene=TFR2
|Chromosome=7
|position=100627408
|Orientation=plus
|GMAF=0.1538
|Gene_s=TFR2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 66.2 | 30.8 | 3.1
| HCB | 79.5 | 18.2 | 2.3
| JPT | 80.9 | 19.1 | 0.0
| YRI | 88.6 | 10.7 | 0.7
| ASW | 86.0 | 14.0 | 0.0
| CHB | 79.5 | 18.2 | 2.3
| CHD | 72.9 | 24.3 | 2.8
| GIH | 74.7 | 24.2 | 1.0
| LWK | 73.1 | 26.9 | 0.0
| MEX | 61.4 | 31.6 | 7.0
| MKK | 70.6 | 28.1 | 1.3
| TSI | 68.0 | 27.8 | 4.1
| HapMapRevision=28
}}{{PMID Auto
|PMID=23751596
|Title=Association between genetic variations in TFR2 gene and coronary heart disease in Chinese: a case-control study
}}

{{ClinVar
|ALT=A
|CAF=0.8462; 0.1538
|CHROM=7
|CLNACC=RCV000020542.1
|CLNALLE=1
|CLNDBN=Hemochromatosis type 3
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1349:C1858664:604250:225123
|CLNHGVS=NC_000007.13:g.100225031G>A
|CLNORIGIN=0
|CLNSIG=2
|CLNSRC=GeneReviews
|CLNSRCID=NBK1349
|COMMON=1
|Disease=Hemochromatosis type 3
|FwdALT=T
|FwdREF=C
|GENEINFO=TFR2:7036
|GENE_ID=7036
|GENE_NAME=TFR2
|REF=G
|RSPOS=100225031
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;PMC;S3D;SLO;VLD;G5;HD;GNO;KGPhase1;KGPilot123;KGPROD;OTHERKG;PH3;LSD
|VC=SNV
|VP=0x05036800000015051f100100
|WGT=0
|dbSNPBuildID=96
|rsid=2075674
}}

{{PMID Auto
|PMID=11102989
|Title=Molecular analysis of the TFR2 gene: report of a novel polymorphism (1878C>T).
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}