The NM_000152.5:c.1630G>A variant in GAA is a missense variant predicted to cause substitution of valine by methionine at amino acid 544 (p.Val544Met). This variant has not been reported in the literature in patients with Pompe disease. The highest population minor allele frequency in gnomAD v2.1.1 is 0.00028 (7/ 24886 alleles) in the African population, which is lower than the ClinGen LSD VCEP’s threshold for PM2_Supporting (<0.001), meeting this criterion. The computational predictor REVEL gives a score of 0.340 which is below the threshold of 0.5, evidence that does not predict a damaging effect on GAA function (BP4). There is a ClinVar entry for this variant (Variation ID: 664232; 2 star review status) with two submitters classifying the variant as a variant of uncertain significance. In summary, this variant meets the criteria to be classified as a variant of uncertain significance for Pompe disease based on the ACMG/AMP criteria applied, as specified by the ClinGen Lysosomal Diseases Variant Curation Expert panel (Specifications Version 2.0): PM3_supporting, BP4. (Classification approved by the ClinGen Lysosomal Diseases Variant Curation Expert Panel on June 6, 2024)