ClinVar Miner

Submissions for variant NM_000059.4(BRCA2):c.9648+15A>C

dbSNP: rs1555289818
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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 RCV000583481 SCV000689215 likely benign Hereditary cancer-predisposing syndrome 2017-06-02 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV005056241 SCV005700093 likely benign Hereditary breast ovarian cancer syndrome 2024-06-10 criteria provided, single submitter clinical testing

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