ClinVar Miner

Submissions for variant NM_005045.4(RELN):c.2895+18A>C

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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 RCV005216471 SCV005852764 likely benign Norman-Roberts syndrome; Familial temporal lobe epilepsy 7 2024-05-26 criteria provided, single submitter clinical testing

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