ClinVar Miner

Submissions for variant NM_007294.4(BRCA1):c.4185+19_4185+38del

dbSNP: rs1597857767
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000874882 SCV001017115 likely benign Hereditary breast ovarian cancer syndrome 2022-07-16 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV001178959 SCV001343527 likely benign Hereditary cancer-predisposing syndrome 2019-07-03 criteria provided, single submitter clinical testing

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