ClinVar Miner

Submissions for variant NM_001350451.2(RBFOX3):c.623-4G>T

gnomAD frequency: 0.00164  dbSNP: rs547643968
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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 RCV000634980 SCV000756358 benign Idiopathic generalized epilepsy 2024-01-17 criteria provided, single submitter clinical testing

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