ClinVar Miner

Submissions for variant NM_005045.4(RELN):c.3663C>T (p.Ser1221=) (rs199705497)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory,University of Chicago RCV000501089 SCV000596746 likely benign not specified 2016-10-05 criteria provided, single submitter clinical testing
Invitae RCV000972007 SCV001119693 likely benign Norman-Roberts syndrome; Epilepsy, familial temporal lobe, 7 2019-12-31 criteria provided, single submitter clinical testing

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