ClinVar Miner

Submissions for variant NM_000059.4(BRCA2):c.7805+17G>A

dbSNP: rs371300428
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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 RCV000197339 SCV000253041 likely benign Hereditary breast ovarian cancer syndrome 2024-08-31 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV003493485 SCV004243064 likely benign not specified 2025-03-04 criteria provided, single submitter clinical testing

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