ClinVar Miner

Submissions for variant NM_000059.4(BRCA2):c.8754+11A>C

dbSNP: rs397508005
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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 RCV002054870 SCV002386991 likely benign Hereditary breast ovarian cancer syndrome 2022-02-01 criteria provided, single submitter clinical testing
ClinVar Staff, National Center for Biotechnology Information (NCBI) RCV000577013 SCV000678835 not provided Familial cancer of breast no assertion provided literature only

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