ClinVar Miner

Submissions for variant NM_058216.3(RAD51C):c.1026+14G>T

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003028314 SCV003308352 likely benign Fanconi anemia complementation group O 2022-02-11 criteria provided, single submitter clinical testing

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