rs995194046

This variant is located in the KLHL7 gene.

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ClinVar annotation

Uncertain Significance★★★☆
2 submitters1 publication

not provided; Inborn genetic diseases

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About KLHL7

This gene encodes a BTB-Kelch-related protein. The encoded protein may be involved in protein degradation. Mutations in this gene have been associated with retinitis pigmentosa 42. [provided by RefSeq, Feb 2010]

View all KLHL7 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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