The NM_000152.5:c.1820G>A variant in GAA is a missense variant predicted to cause substitution of glycine by aspartic acid at amino acid 607 (p.Gly607Asp). Four probands with symptoms consistent with infantile-onset-Pompe disease have been reported with this variant (PMID: 29889338, 33301762, 37087815), three with documented deficiency of GAA activity (PMID: 33301762, 37097815) (PP4_Moderate). All of these probands are homozygous this variant. This variant is absent in both gnomAD 2.1.1 and 4.0.0 (PM2_Supporting). Expression of the variant in COS-7 cells resulted 2% wild-type GAA activity in one study (PMID: 14695532) and <2% wild-type GAA activity in a separate study (PMID: 19862843) (PS3_Moderate). The computational predictor REVEL gives a score of 0.872 which is above the threshold predicting a damaging (>0.7) or benign (<0.5) impact on GAA function. Two other missense variants, c.1819G>T (p.Gly607Cys) (ClinVar Variation ID: 2118057) and c.1819G>A (p.Gly607Ser) (ClinVar Variation ID: 456385), in the same codon have been reported in patients with Pompe disease. However, these variants have not been classified by the ClinGen Lysosomal Diseases VCEP and, therefore, this evidence is not sufficient to meet PM5 at any strength. There is a ClinVar entry for this variant (Variation ID: 932221). In summary, this variant meets the criteria to be classified as Likely Pathogenic for Pompe disease. GAA-specific ACMG/AMP criteria met, based on specifications of the ClinGen Lysosomal Diseases VCEP (Specifications Version 2.0): PM3, PS3_Moderate, PP4_Moderate, PM2_Supporting, PP3). (Classification approved by the ClinGen Lysosomal Diseases Variant Curation Expert Panel on April 2, 2024)