| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (synonymous variant +1 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (synonymous variant +1 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (synonymous variant +1 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Indel (missense variant +1 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (synonymous variant +1 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (missense variant +1 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (intron variant) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Deletion (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Insertion (intron variant) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (missense variant +2 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (synonymous variant +2 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (synonymous variant +2 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (missense variant +2 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (missense variant +2 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (missense variant +2 more) | HNRNPDL-related myopathy with protein aggregates and rimmed vacuoles +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +2 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +2 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (missense variant +2 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (synonymous variant +2 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (missense variant +2 more) | not provided | |
| | | Single nucleotide variant (missense variant +2 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (missense variant +2 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +2 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (synonymous variant +2 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (missense variant +2 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (missense variant +2 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G +1 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (intron variant +2 more) | not provided +1 more | |
| | | Single nucleotide variant (intron variant) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (intron variant) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Duplication (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (intron variant) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (intron variant) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (intron variant) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (synonymous variant +1 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (missense variant +1 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Deletion (inframe_deletion +1 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (missense variant +1 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (missense variant +1 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (missense variant +1 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (missense variant +1 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (synonymous variant +1 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (synonymous variant +1 more) | HNRNPDL-related disorder +1 more | |
| | | Microsatellite (inframe_deletion +1 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (synonymous variant +1 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (synonymous variant +1 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Microsatellite (inframe_deletion +1 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (nonsense +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Deletion (frameshift variant +1 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (synonymous variant +1 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (missense variant +1 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (synonymous variant +1 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (missense variant +1 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (missense variant +1 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (intron variant) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (intron variant) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Deletion (intron variant) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (intron variant) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (intron variant) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (intron variant) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (intron variant) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (missense variant +1 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (synonymous variant +1 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (synonymous variant +1 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (missense variant +1 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (synonymous variant +1 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (synonymous variant +1 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Deletion (inframe_deletion +1 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (synonymous variant +1 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (missense variant +1 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (missense variant +1 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (synonymous variant +1 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (synonymous variant +1 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (synonymous variant +1 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Indel (missense variant +1 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Deletion (frameshift variant +1 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (missense variant +1 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (missense variant +1 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (missense variant +1 more) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (intron variant) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (intron variant) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (intron variant) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (intron variant) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |
| | | Single nucleotide variant (intron variant) | Autosomal dominant limb-girdle muscular dystrophy type 1G | |