The NM_000152.5:c.2510G>A variant in GAA is a missense variant predicted to cause substitution of Arginine by Histidine at amino acid 837 (p.Arg837His). The highest population minor allele frequency in gnomAD v2.1.1 is 0.00019 (3/16178 alleles) in the African population, which is lower than the ClinGen Lysosomal Diseases VCEP’s threshold for PM2_Supporting (<0.001), meeting this criterion (PM2_Supporting). The computational predictor REVEL gives a score of 0.845 which is above the threshold of 0.7, evidence that correlates with impact to GAA function (PP3). This variant has been detected in at least 3 individuals, but not with a pathogenic or likely pathogenic variant. Also, no symptoms of Pompe disease were described for any of the individuals (PMID: 27711114, internal laboratory data). Therefore, this does not meet PM3 or PP4. There is a ClinVar entry for this variant (Variation ID: 284232, 2 star review status) with 6 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): PM2_Supporting, PP3. (Classification approved by the ClinGen Lysosomal Diseases Variant Curation Expert Panel on October 8, 2023).