The NM_000152.5:c.1847dup (p.Asp616GlufsTer20) variant in GAA is a frameshift variant predicted to cause a premature stop codon in exon 14 out of a total of 20 exons, leading to nonsense mediated decay in a gene in which loss-of-function is an established disease mechanism (PVS1). The highest population minor allele frequency in gnomAD v4.1.0. is 0.000003391 (4/1179640 alleles) in the European non-Finnish population, which is lower than the ClinGen LD VCEP's threshold (<0.001) for PM2_Supporting, meeting this criterion (PM2_Supporting). The variant was identified in a French patient with late onset Pompe disease (PMID 30155607). However, no clinical or laboratory information about the patient, such symptoms, residual GAA activity, or second variant, were provided (PM3_Not Met, PP4_Not Met). There is a ClinVar entry for this variant (Variation ID: 693996). In summary, this variant meets the criteria to be classified as likely pathogenic for Pompe disease. The classification of this variant has been upgraded from Variant of Uncertain Significance to Likely Pathogenic based on the recommendations of the ClinGen Sequence Variant Interpretation Working Group, that a variant meeting PVS1 and PM2_Supporting is classified as Likely Pathogenic (https://clinicalgenome.org/site/assets/files/5182/pm2_-_svi_recommendation_-_approved_sept2020.pdf ) GAA-specific ACMG/AMP criteria applied, as specified by the ClinGen Lysosomal Diseases VCEP (Specifications Version 2.0): PVS1, PM2_Supporting. (Classification approved by the ClinGen Lysosomal Diseases VCEP on April 9, 2026)