ClinVar Miner

Submissions for variant NM_005045.4(RELN):c.227-26dup

dbSNP: rs561211301
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001567341 SCV001791005 likely benign not provided 2019-08-10 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002072178 SCV002404481 benign Norman-Roberts syndrome; Familial temporal lobe epilepsy 7 2025-01-20 criteria provided, single submitter clinical testing

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