ClinVar Miner

Submissions for variant NM_000059.4(BRCA2):c.6043T>C (p.Leu2015=)

dbSNP: rs1566233782
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV000773622 SCV000907316 likely benign Hereditary cancer-predisposing syndrome 2018-07-31 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000985556 SCV001133850 uncertain significance not provided 2019-06-16 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003645102 SCV004396586 likely benign Hereditary breast ovarian cancer syndrome 2023-11-20 criteria provided, single submitter clinical testing

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