| | | Single nucleotide variant (missense variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Microsatellite (inframe_deletion) | PCK1-related disorder | |
| | | Single nucleotide variant (intron variant) | PCK1-related disorder | |
| | | Single nucleotide variant (missense variant) | Phosphoenolpyruvate carboxykinase deficiency, cytosolic +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | PCK1-related disorder | |
| | | Single nucleotide variant (intron variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | PCK1-related disorder | |
| | | Single nucleotide variant (synonymous variant) | PCK1-related disorder +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | PCK1-related disorder | |
| | | Single nucleotide variant (synonymous variant) | PCK1-related disorder +1 more | |
| | | Single nucleotide variant (synonymous variant) | PCK1-related disorder | |
| | | Single nucleotide variant (synonymous variant) | PCK1-related disorder +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | | Single nucleotide variant (intron variant) | Inborn genetic diseases +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Phosphoenolpyruvate carboxykinase deficiency, cytosolic +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +2 more | GConflicting classifications of pathogenicity |