ClinVar Miner

Submissions for variant NM_018723.4(RBFOX1):c.931-20_931-19inv

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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 RCV003011410 SCV003300767 uncertain significance Idiopathic generalized epilepsy 2022-08-01 criteria provided, single submitter clinical testing Experimental studies and prediction algorithms are not available or were not evaluated, and the effect of this variant on mRNA splicing is currently unknown. In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. This variant has not been reported in the literature in individuals affected with RBFOX1-related conditions. Information on the frequency of this variant in the gnomAD database is not available, as this variant may be reported differently in the database. This sequence change falls in intron 10 of the RBFOX1 gene. It does not directly change the encoded amino acid sequence of the RBFOX1 protein.

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