ClinVar Miner

Submissions for variant NM_000059.4(BRCA2):c.2989T>C (p.Leu997=)

dbSNP: rs2072469851
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001189083 SCV001356287 likely benign Hereditary cancer-predisposing syndrome 2019-12-10 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV005093975 SCV005764512 likely benign Hereditary breast ovarian cancer syndrome 2024-07-24 criteria provided, single submitter clinical testing

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