ClinVar Miner

Submissions for variant NM_007294.4(BRCA1):c.96G>A (p.Lys32=)

gnomAD frequency: 0.00001  dbSNP: rs1597912013
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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 RCV001399462 SCV001601252 likely benign Hereditary breast ovarian cancer syndrome 2019-06-28 criteria provided, single submitter clinical testing
Brotman Baty Institute, University of Washington RCV001076967 SCV001242820 not provided Breast-ovarian cancer, familial, susceptibility to, 1 no assertion provided in vitro

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