ClinVar Miner

Submissions for variant NM_005045.4(RELN):c.77C>T (p.Ala26Val) (rs144557847)

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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics, Eurofins Clinical Diagnostics RCV000173363 SCV000224465 likely benign not specified 2017-02-22 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV000173363 SCV000596752 uncertain significance not specified 2015-12-31 criteria provided, single submitter clinical testing
Invitae RCV001080868 SCV000656358 likely benign Norman-Roberts syndrome; Epilepsy, familial temporal lobe, 7 2020-11-22 criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000556641 SCV001145265 benign not provided 2018-11-23 criteria provided, single submitter clinical testing
GeneDx RCV000556641 SCV001791409 likely benign not provided 2020-09-10 criteria provided, single submitter clinical testing

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