ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.10094_10095insGAATTATATC (p.Ser3366fs) (rs1064792995)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000459760 SCV000560505 benign Hereditary breast and ovarian cancer syndrome 2017-07-24 criteria provided, single submitter clinical testing
Fulgent Genetics,Fulgent Genetics RCV000487571 SCV000575728 likely benign Breast-ovarian cancer, familial 2 2015-08-17 criteria provided, single submitter clinical testing
Color RCV000771163 SCV000903044 likely benign Hereditary cancer-predisposing syndrome 2018-01-10 criteria provided, single submitter clinical testing

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