ClinVar Miner

Submissions for variant NM_000059.4(BRCA2):c.8488-20T>G

dbSNP: rs1593930846
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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 RCV000845284 SCV001678658 likely benign Hereditary breast ovarian cancer syndrome 2020-09-03 criteria provided, single submitter clinical testing
Hereditary Cancer Genetics group, Vall d'Hebron Institute of Oncology RCV000845284 SCV000916372 benign Hereditary breast ovarian cancer syndrome 2019-03-01 no assertion criteria provided research

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