ClinVar Miner

Submissions for variant NM_007294.4(BRCA1):c.21C>G (p.Arg7=)

dbSNP: rs149402012
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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 RCV001504317 SCV001709193 likely benign Hereditary breast ovarian cancer syndrome 2019-11-20 criteria provided, single submitter clinical testing
Brotman Baty Institute, University of Washington RCV001072329 SCV001237689 not provided Breast-ovarian cancer, familial, susceptibility to, 1 no assertion provided in vitro

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