ClinVar Miner

Submissions for variant NM_001350451.2(RBFOX3):c.622+3dup

dbSNP: rs1351338220
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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 RCV001510803 SCV001717935 benign Idiopathic generalized epilepsy 2022-08-23 criteria provided, single submitter clinical testing

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