ClinVar Miner

Submissions for variant NM_018723.4(RBFOX1):c.562-15T>A

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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 RCV002947894 SCV003271559 likely benign Idiopathic generalized epilepsy 2022-01-10 criteria provided, single submitter clinical testing

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