Gene entry
TFR2
transferrin receptor 2
- Chromosome
- 7
- Cytoband
- 7q22.1
- Variants (rsID)
- 13
TFR2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 7 (region 7q22.1). Its official name is “transferrin receptor 2”. The reference table lists 13 variants (rsID) for this gene.
Clinically classified variants
7 reference-table entries with clinical significance.
- rs35704760Benignsingle nucleotide variantHemochromatosis type 3|Hereditary hemochromatosis
- rs41295899Benignsingle nucleotide variantHereditary hemochromatosis|Hemochromatosis type 3
- rs41295942Benignsingle nucleotide variantHereditary hemochromatosis|Hemochromatosis type 3
- rs141140309Conflicting interpretationssingle nucleotide variantHereditary hemochromatosis|Hemochromatosis type 3
- rs187119131Likely benignsingle nucleotide variantHereditary hemochromatosis
- rs200053955Uncertain significancesingle nucleotide variantHereditary hemochromatosis|Hemochromatosis type 3
- rs80338885Uncertain significancesingle nucleotide variantHemochromatosis type 3|Hereditary hemochromatosis
Other listed variants
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.