ClinVar Miner

Submissions for variant NM_000742.4(CHRNA2):c.15T>A (p.Cys5Ter)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Revvity Omics, Revvity RCV003144924 SCV003832048 uncertain significance Autosomal dominant nocturnal frontal lobe epilepsy 4 2020-03-23 criteria provided, single submitter clinical testing

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