ClinVar Miner

Submissions for variant NM_018723.4(RBFOX1):c.415-14C>T

dbSNP: rs766827645
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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 RCV002174832 SCV002348675 likely benign Idiopathic generalized epilepsy 2021-11-16 criteria provided, single submitter clinical testing

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