ClinVar Miner

Submissions for variant NM_032043.3(BRIP1):c.1794+7T>G

dbSNP: rs2145089607
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001965672 SCV002242368 likely benign Familial cancer of breast; Fanconi anemia complementation group J 2022-12-24 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV004785418 SCV005402949 likely benign Familial cancer of breast 2024-08-29 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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