ClinVar Miner

Submissions for variant NM_005045.4(RELN):c.2003-19C>G

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002606688 SCV003503166 likely benign Norman-Roberts syndrome; Familial temporal lobe epilepsy 7 2022-02-20 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004704881 SCV005228467 likely benign not provided criteria provided, single submitter not provided

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