ClinVar Miner

Submissions for variant NM_001350451.2(RBFOX3):c.568+17C>T

gnomAD frequency: 0.26012  dbSNP: rs11651975
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001656785 SCV001865571 benign not provided 2019-01-22 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002073016 SCV002408808 benign Idiopathic generalized epilepsy 2024-02-01 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001656785 SCV005255675 benign not provided criteria provided, single submitter not provided

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