ClinVar Miner

Submissions for variant NC_000003.11:g.(?_81584336)_(81810678_?)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 RCV001389914 SCV001591438 pathogenic Glycogen storage disease, type IV; Glycogen storage disease IV, classic hepatic 2021-01-08 criteria provided, single submitter clinical testing This variant is a gross deletion of the genomic region encompassing exon(s) 1-14 of the GBE1 gene, which includes the initiator codon. The 5' end of this event is unknown as it extends beyond the assayed region for this gene and therefore may encompass additional genes. The 3' boundary is likely confined to intron 14 of the GBE1 gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in GBE1 are known to be pathogenic (PMID: 15452297, 20058079). This variant has not been reported in the literature in individuals with GBE1-related conditions. For these reasons, this variant has been classified as Pathogenic.

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