ClinVar Miner

Submissions for variant NM_000059.4(BRCA2):c.1002_1003dup (p.Glu335fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Greenwood Genetic Center Diagnostic Laboratories, Greenwood Genetic Center RCV003233393 SCV003932219 likely pathogenic Hereditary breast ovarian cancer syndrome 2023-03-23 criteria provided, single submitter clinical testing PVS1, PM2

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