ClinVar Miner

Submissions for variant NM_007294.4(BRCA1):c.4986+7G>A

dbSNP: rs2052352092
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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 RCV002557938 SCV003325697 likely benign Hereditary breast ovarian cancer syndrome 2022-03-11 criteria provided, single submitter clinical testing
Brotman Baty Institute, University of Washington RCV001077881 SCV001243882 not provided Breast-ovarian cancer, familial, susceptibility to, 1 no assertion provided in vitro

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