ClinVar Miner

Submissions for variant NM_007294.4(BRCA1):c.5407-13C>A

dbSNP: rs761772657
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001185952 SCV001352270 uncertain significance Hereditary cancer-predisposing syndrome 2019-02-06 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002554650 SCV002991191 likely benign Hereditary breast ovarian cancer syndrome 2021-12-09 criteria provided, single submitter clinical testing
Brotman Baty Institute, University of Washington RCV001073204 SCV001238719 not provided Breast-ovarian cancer, familial, susceptibility to, 1 no assertion provided in vitro

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