ClinVar Miner

Submissions for variant NM_002878.4(RAD51D):c.145-16_145-15del

dbSNP: rs1555570314
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000615705 SCV000732741 likely benign not specified 2017-06-14 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Color Diagnostics, LLC DBA Color Health RCV001525243 SCV001735292 likely benign Hereditary cancer-predisposing syndrome 2021-01-21 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002066893 SCV002350681 likely benign Breast-ovarian cancer, familial, susceptibility to, 4 2024-11-19 criteria provided, single submitter clinical testing

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