rs750977682

This variant is located in the SDCCAG8 gene.

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ClinVar annotation

Uncertain Significance★★★☆
3 submitters1 publication

Bardet-Biedl syndrome 16;Senior-Loken syndrome 7; SDCCAG8-related disorder; Inborn genetic diseases

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About SDCCAG8

This gene encodes a centrosome associated protein. This protein may be involved in organizing the centrosome during interphase and mitosis. Mutations in this gene are associated with retinal-renal ciliopathy. [provided by RefSeq, Oct 2010]

View all SDCCAG8 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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