rs1461496815

This variant is located in the TFRC gene.

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ClinVar annotation

Conflicting Classifications
2 submitters1 publication

not provided; Inborn genetic diseases

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About TFRC

This gene encodes a cell surface receptor necessary for cellular iron uptake by the process of receptor-mediated endocytosis. This receptor is required for erythropoiesis and neurologic development. Multiple alternatively spliced variants have been identified. [provided by RefSeq, Sep 2015]

View all TFRC variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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