ClinVar Miner

Submissions for variant NC_000017.11:g.(?_80109935)_(80113376_?)del

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001032590 SCV001195897 pathogenic Glycogen storage disease, type II 2021-12-01 criteria provided, single submitter clinical testing For these reasons, this variant has been classified as Pathogenic. This variant has not been reported in the literature in individuals affected with GAA-related conditions. This variant is a gross deletion of the genomic region encompassing exon(s) 9-15 of the GAA gene. This deletion is out-of-frame, and is expected to create a premature termination codon and result in an absent or disrupted protein product. Loss-of-function variants in GAA are known to be pathogenic (PMID: 18425781, 22252923).

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