ClinVar Miner

Submissions for variant NM_007294.4(BRCA1):c.301+146A>C

gnomAD frequency: 0.00039  dbSNP: rs571713225
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV003492082 SCV004232601 likely benign Hereditary cancer 2024-01-23 criteria provided, single submitter clinical testing
Department of Pathology and Laboratory Medicine, Sinai Health System RCV000502494 SCV000591255 uncertain significance not provided no assertion criteria provided clinical testing

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