ClinVar Miner

Submissions for variant NM_005045.4(RELN):c.4872A>G (p.Gln1624=) (rs149121159)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics, Eurofins Clinical Diagnostics RCV000723997 SCV000229668 uncertain significance not provided 2014-07-04 criteria provided, single submitter clinical testing
Genetic Services Laboratory,University of Chicago RCV000177747 SCV000596745 uncertain significance not specified 2015-12-28 criteria provided, single submitter clinical testing
Invitae RCV001088410 SCV001037552 likely benign Norman-Roberts syndrome; Epilepsy, familial temporal lobe, 7 2019-12-31 criteria provided, single submitter clinical testing

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