ClinVar Miner

Submissions for variant NM_005045.4(RELN):c.6642G>A (p.Met2214Ile)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Dr. med. U. Finckh, Human Genetics, Eurofins MVZ RCV003234852 SCV003932821 uncertain significance Familial temporal lobe epilepsy 7 criteria provided, single submitter clinical testing

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