rs59115933

This variant is located in the BRIP1 gene.

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ClinVar annotation

Benign★☆☆☆

1 submitter

Fanconi anemia complementation group J

About BRIP1

The protein encoded by this gene is a member of the RecQ DEAH helicase family and interacts with the BRCT repeats of breast cancer, type 1 (BRCA1). The bound complex is important in the normal double-strand break repair function of breast cancer, type 1 (BRCA1). This gene may be a target of germline cancer-inducing mutations. [provided by RefSeq, Jul 2008]

View all BRIP1 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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