ClinVar Miner

Submissions for variant NM_018723.4(RBFOX1):c.677-4G>A

gnomAD frequency: 0.00003  dbSNP: rs759738790
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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 RCV000634994 SCV000756372 likely benign Idiopathic generalized epilepsy 2023-10-03 criteria provided, single submitter clinical testing

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