ClinVar Miner

Submissions for variant NM_032043.3(BRIP1):c.508-18T>C

dbSNP: rs1555615801
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV000584357 SCV000689399 likely benign Hereditary cancer-predisposing syndrome 2015-09-08 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV004787991 SCV005406899 likely benign Familial cancer of breast 2024-08-21 criteria provided, single submitter clinical testing This variant is considered likely benign. This variant is intronic and is not expected to impact mRNA splicing.

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