ClinVar Miner

Submissions for variant NM_002878.4(RAD51D):c.346-7C>T

dbSNP: rs1060504768
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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 RCV000463044 SCV000561573 likely benign Breast-ovarian cancer, familial, susceptibility to, 4 2024-11-11 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV000775732 SCV000910157 likely benign Hereditary cancer-predisposing syndrome 2018-05-03 criteria provided, single submitter clinical testing

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