ClinVar Miner

Submissions for variant NM_005045.4(RELN):c.9370-13_9370-8del

dbSNP: rs141397961
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000081250 SCV000113158 benign not specified 2013-04-22 criteria provided, single submitter clinical testing
Invitae RCV000558845 SCV000656375 benign Norman-Roberts syndrome; Familial temporal lobe epilepsy 7 2024-02-01 criteria provided, single submitter clinical testing
GeneDx RCV001719840 SCV000729736 benign not provided 2018-05-03 criteria provided, single submitter clinical testing

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