| | | Single nucleotide variant (3 prime UTR variant) | GGCX-related condition | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | | Single nucleotide variant (intron variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | GGCX-related condition | |
| | | Single nucleotide variant (synonymous variant) | Vitamin K-dependent clotting factors, combined deficiency of, type 1 +2 more | |
| | | Single nucleotide variant (intron variant) | GGCX-related condition | |
| | | Single nucleotide variant (missense variant) | GGCX-related condition +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (nonsense) | GGCX-related condition +1 more | GPathogenic/Likely pathogenic |
| | | Microsatellite (frameshift variant) | GGCX-related condition +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (synonymous variant) | GGCX-related condition +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (nonsense) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | GGCX-related condition +1 more | |
| | | Single nucleotide variant (intron variant) | GGCX-related condition +1 more | |
| | | Single nucleotide variant (synonymous variant) | GGCX-related condition +2 more | |
| | | Single nucleotide variant (missense variant) | GGCX-related condition +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | GGCX-related condition | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +2 more | |
| | | Single nucleotide variant (synonymous variant) | GGCX-related condition +1 more | |