The variant NM_000540.3(RYR1):c.10348-6C>G in RYR1 is an intronic variant located in intron 68. The filtering allele frequency is 0.0003329 (34/75078 alleles, 0 homozygotes) for the African/African American population, which meets no codes. In addition, the SpliceAI Acceptor Loss value is 0.47. The variant was found in compound heterozygosity with variants of uncertain significance, likely pathogenic, or pathogenic variants in 22 patients (PM3_Very Strong; PMIDs: 18253926, 21062345, 20839240, 23553484, 28818389, 30932294, 31069529, 30611313, 34440373, 35627144, 35616356, 36939041). At least 3 patients with this variant displayed ophthalmoparesis and presence of cores on muscle biopsy, which is highly specific for RYR1-related myopathy (PP4; PMID: 20839240). This variant has been observed in at least 11 South African patients with RYR1-related myopathy, suggesting a possible founder variant (PMID: 20839240). The variant has also been reported in cis with the c.14524G>A (p.Val4842Met) variant in 17 of the 22 probands, which is part of a known haplotype and has been reported as a compound heterozygous change in individuals with RYR1-related myopathies (PMIDs: 18253926, 21062345, 20839240, 23553484, 30932294, 30611313, 35627144). The variant has been found to segregate with disease in 4 affected relatives from 2 families (PP1; PMIDs: 18253926, 21062345). Functional studies in patient cells showed that the variant resulted in a loss of splicing of intron 68 and the introduction of a premature stop codon causing the mRNA to undergo NMD (PMIDs: 18253926, 25525159) (PS3_Supporting). In summary, this variant meets the criteria to be classified as pathogenic for autosomal recessive RYR1-related myopathy based on the ACMG/AMP criteria applied, as specified by the ClinGen Congenital Myopathies VCEP: PM3_Very Strong, PP4, PP1, PS3_Supporting (ClinGen Congenital Myopathies VCEP specifications version 2; May 19th, 2025).