ClinVar Miner

Submissions for variant NM_006030.4(CACNA2D2):c.405+7G>A

dbSNP: rs2106891509
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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 RCV002137211 SCV002411635 likely benign Early infantile epileptic encephalopathy with suppression bursts 2021-09-02 criteria provided, single submitter clinical testing

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