ClinVar Miner

Submissions for variant NM_005045.4(RELN):c.4191C>T (p.Asn1397=) (rs544646610)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics, Eurofins Clinical Diagnostics RCV000592715 SCV000707711 uncertain significance not provided 2017-05-02 criteria provided, single submitter clinical testing
Invitae RCV000653043 SCV000774917 likely benign Norman-Roberts syndrome; Epilepsy, familial temporal lobe, 7 2019-12-31 criteria provided, single submitter clinical testing

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