ClinVar Miner

Submissions for variant NM_005045.4(RELN):c.4937-4del

dbSNP: rs35268159
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000177789 SCV000229721 benign not specified 2014-07-17 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001511697 SCV001718982 benign Norman-Roberts syndrome; Familial temporal lobe epilepsy 7 2025-01-25 criteria provided, single submitter clinical testing
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen RCV000610154 SCV000734538 benign Norman-Roberts syndrome no assertion criteria provided clinical testing
Clinical Genetics, Academic Medical Center RCV000177789 SCV001920804 benign not specified no assertion criteria provided clinical testing

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