The c.704T>G variant in the glucokinase gene, GCK, causes an amino acid change of methionine to arginine at codon 235 (p.(Met235Arg)) of NM_000162.5. GCK is defined by the ClinGen MDEP as a gene that has a low rate of benign missense variation and has pathogenic missense variants as a common mechanism of disease (PP2). This variant is predicted to be deleterious by computational evidence, with a REVEL score of 0.934, which is greater than the MDEP VCEP threshold of 0.70 (PP3). This variant is absent from gnomAD v4.1.0 (PM2_Supporting). Two other missense variants at the same residue, c.704T>C (p.Met235Thr) and c.703A>G (p.Met235Val), have been interpreted as pathogenic by the ClinGen MDEP, and p.Met235Arg has a greater Grantham distance than both of these variants (PM5_Strong). This variant was identified in an individual with a phenotype suggestive of GCK-hyperglycemia; however, PP4 is unable to be evaluated due to insufficient clinical information (internal lab contributors). In summary, c.704T>G meets the criteria to be classified as likely pathogenic for monogenic diabetes. ACMG/AMP criteria applied, as specified by the ClinGen MDEP (specification version 3.1.0, approved 10/10/2025): PM5_Strong, PM2_Supporting, PP2, PP3.