ClinVar Miner

Submissions for variant NC_000016.10:g.(?_2048596)_(2098004_?)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 RCV001033917 SCV001197224 pathogenic Tuberous sclerosis 2 2019-05-29 criteria provided, single submitter clinical testing A gross deletion of the genomic region encompassing the full coding sequence of the TSC2 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. Loss-of-function variants in TSC2 are known to be pathogenic. This particular variant has been reported in the literature in individuals affected with tuberous sclerosis complex (PMID: 17287951, 16114042). For these reasons, this variant has been classified as Pathogenic.

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