ClinVar Miner

Submissions for variant NM_007294.4(BRCA1):c.5277+2916_5277+2946del

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Department of Pathology and Laboratory Medicine, Sinai Health System RCV005396397 SCV006058352 likely pathogenic Familial cancer of breast; Breast-ovarian cancer, familial, susceptibility to, 1; Fanconi anemia, complementation group S criteria provided, single submitter clinical testing

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