ClinVar Miner

Submissions for variant NM_058216.3(RAD51C):c.145+17G>T

dbSNP: rs369854656
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000611158 SCV000732440 likely benign not specified 2017-05-26 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.
Labcorp Genetics (formerly Invitae), Labcorp RCV002066866 SCV002422204 likely benign Fanconi anemia complementation group O 2025-01-08 criteria provided, single submitter clinical testing

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