ClinVar Miner

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

dbSNP: rs112339093
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000475990 SCV000561094 benign Idiopathic generalized epilepsy 2024-01-15 criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV001662443 SCV001880735 benign not specified 2021-03-19 criteria provided, single submitter clinical testing

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