ClinVar Miner

Submissions for variant NM_000059.4(BRCA2):c.8331+15A>T

dbSNP: rs550087774
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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 RCV001188704 SCV001355837 likely benign Hereditary cancer-predisposing syndrome 2018-11-06 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002560932 SCV003487874 likely benign Hereditary breast ovarian cancer syndrome 2024-07-03 criteria provided, single submitter clinical testing

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