rs747725530

This variant is located in the FOXC2 gene.

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ClinVar annotation

Uncertain Significance★☆☆☆
1 submitter

Inborn genetic diseases

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About FOXC2

This gene belongs to the forkhead family of transcription factors which is characterized by a distinct DNA-binding forkhead domain. The specific function of this gene has not yet been determined; however, it may play a role in the development of mesenchymal tissues. [provided by RefSeq, Jul 2008]

View all FOXC2 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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