ClinVar Miner

Submissions for variant NM_018723.4(RBFOX1):c.758-4G>T

dbSNP: rs112339093
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000475990 SCV000561094 benign Idiopathic generalized epilepsy 2024-01-15 criteria provided, single submitter clinical testing
Athena Diagnostics RCV001662443 SCV001880735 benign not specified 2021-03-19 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004716507 SCV005296539 benign not provided criteria provided, single submitter not provided

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