ClinVar Miner

Submissions for variant NC_000003.12:g.(?_81490397)_(81761527_?)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 RCV001033100 SCV001196407 pathogenic Glycogen storage disease, type IV; Glycogen storage disease IV, classic hepatic 2022-08-20 criteria provided, single submitter clinical testing A gross deletion of the genomic region encompassing the full coding sequence of the GBE1 gene has been identified. Loss-of-function variants in GBE1 are known to be pathogenic (PMID: 15452297, 20058079). The boundaries of this event are unknown as they extend beyond the assayed region for this gene and therefore may encompass additional genes. This variant has not been reported in the literature in individuals affected with GBE1-related conditions. For these reasons, this variant has been classified as Pathogenic.

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