ClinVar Miner

Submissions for variant NM_002878.4(RAD51D):c.346-19C>T

dbSNP: rs1567728479
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV000773955 SCV000907655 likely benign Hereditary cancer-predisposing syndrome 2018-09-26 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002068509 SCV002447861 likely benign Breast-ovarian cancer, familial, susceptibility to, 4 2024-09-09 criteria provided, single submitter clinical testing

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