ClinVar Miner

Submissions for variant NM_005045.4(RELN):c.4374C>T (p.Leu1458=)

dbSNP: rs1584308677
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001393199 SCV001594855 likely benign Norman-Roberts syndrome; Familial temporal lobe epilepsy 7 2021-12-30 criteria provided, single submitter clinical testing

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