ClinVar Miner

Submissions for variant NM_032043.3(BRIP1):c.*6C>G

dbSNP: rs1567727060
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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 RCV000774080 SCV000907780 uncertain significance Hereditary cancer-predisposing syndrome 2019-05-02 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV004788173 SCV005404596 benign Familial cancer of breast 2024-09-25 criteria provided, single submitter clinical testing This variant is considered benign. This variant occurs in the non-coding 3' untranslated region of the gene, and is not expected to impact protein function.

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