ClinVar Miner

Submissions for variant NM_001350451.2(RBFOX3):c.360+12C>T

gnomAD frequency: 0.00004  dbSNP: rs901701800
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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 RCV002220272 SCV002368169 likely benign Idiopathic generalized epilepsy 2022-02-05 criteria provided, single submitter clinical testing

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