ClinVar Miner

Submissions for variant NM_000059.4(BRCA2):c.5421T>C (p.Asp1807=)

dbSNP: rs1421290001
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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 RCV002193464 SCV002483361 likely benign Hereditary breast ovarian cancer syndrome 2025-01-06 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV003585227 SCV004362106 likely benign Hereditary cancer-predisposing syndrome 2023-10-09 criteria provided, single submitter clinical testing

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