ClinVar Miner

Submissions for variant NM_000059.4(BRCA2):c.7761C>T (p.Leu2587=)

dbSNP: rs1555286446
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000541855 SCV000635601 likely benign Hereditary breast ovarian cancer syndrome 2023-10-30 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV001178554 SCV001343020 likely benign Hereditary cancer-predisposing syndrome 2019-11-06 criteria provided, single submitter clinical testing

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