rs759725355

This variant is located in the FRZB gene.

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ClinVar annotation

Uncertain Significance★☆☆☆

1 submitter

not specified

About FRZB

The protein encoded by this gene is a secreted protein that is involved in the regulation of bone development. Defects in this gene are a cause of female-specific osteoarthritis (OA) susceptibility. [provided by RefSeq, Apr 2010]

View all FRZB variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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