ClinVar Miner

Submissions for variant NM_005045.4(RELN):c.2466-7dup

dbSNP: rs571882672
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ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000176080 SCV000227676 benign not specified 2014-07-14 criteria provided, single submitter clinical testing
Athena Diagnostics RCV000176080 SCV000614861 benign not specified 2016-10-28 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001517303 SCV001725781 benign Norman-Roberts syndrome; Familial temporal lobe epilepsy 7 2024-01-08 criteria provided, single submitter clinical testing

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