ClinVar Miner

Submissions for variant NM_005097.4(LGI1):c.838+10G>A

gnomAD frequency: 0.00001  dbSNP: rs756267808
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV002231766 SCV000639385 likely benign Autosomal dominant epilepsy with auditory features 2023-05-25 criteria provided, single submitter clinical testing

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