ClinVar Miner

Submissions for variant NM_005045.4(RELN):c.2016G>A (p.Pro672=) (rs146749232)

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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 RCV000175186 SCV000226627 uncertain significance not provided 2014-05-09 criteria provided, single submitter clinical testing
Invitae RCV001088118 SCV000774913 likely benign Norman-Roberts syndrome; Epilepsy, familial temporal lobe, 7 2019-12-31 criteria provided, single submitter clinical testing

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