ClinVar Miner

Submissions for variant NM_002878.4(RAD51D):c.264-6C>T

dbSNP: rs1567728794
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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 RCV001183593 SCV001349384 uncertain significance Hereditary cancer-predisposing syndrome 2019-02-04 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001470913 SCV001675012 likely benign Breast-ovarian cancer, familial, susceptibility to, 4 2024-08-01 criteria provided, single submitter clinical testing

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