ClinVar Miner

Submissions for variant NC_000008.10:g.(?_133141509)_(133492779_?)del

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001383837 SCV001583126 pathogenic Benign neonatal seizures 2020-06-01 criteria provided, single submitter clinical testing A gross deletion of the genomic region encompassing the full coding sequence of the KCNQ3 gene has been identified. The boundaries of this event are unknown as the deletion extends beyond the assayed region for this gene and therefore may encompass additional genes. This variant has not been reported in the literature in individuals with KCNQ3-related conditions. Loss-of-function variants in KCNQ3 are known to be pathogenic (PMID: 29383681, 29852413). For these reasons, this variant has been classified as Pathogenic.

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