ClinVar Miner

Submissions for variant NM_000059.4(BRCA2):c.9117+17G>T

dbSNP: rs1477754012
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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 RCV000937890 SCV001083684 likely benign Hereditary breast ovarian cancer syndrome 2024-11-19 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV005236459 SCV005884042 likely benign not specified 2024-12-11 criteria provided, single submitter clinical testing

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