| | | Single nucleotide variant (missense variant +1 more) | not provided +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Osteogenesis imperfecta +5 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Osteogenesis imperfecta +8 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Adult hypophosphatasia +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not provided +4 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | Adult hypophosphatasia +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not provided +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | ALPL-related disorder +6 more | |
| | | Single nucleotide variant (missense variant) | Hypophosphatasia +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (splice donor variant) | not provided +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Osteogenesis imperfecta +6 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Hypophosphatasia +1 more | |
| | | Single nucleotide variant (missense variant) | Hypophosphatasia +4 more | GPathogenic/Likely pathogenic |
| | | Deletion (frameshift variant) | not provided +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Deficiency of aromatic-L-amino-acid decarboxylase | |
| | | Single nucleotide variant (intron variant) | Deficiency of aromatic-L-amino-acid decarboxylase +1 more | |
| | | Single nucleotide variant (non-coding transcript variant +2 more) | Deficiency of aromatic-L-amino-acid decarboxylase | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +4 more | |
| | | Single nucleotide variant (nonsense) | Arrhythmogenic right ventricular dysplasia, familial, 15 | |
| | FLNC, FLNC-AS1 (D2670fs +1 more) | Deletion (frameshift variant) | not provided +5 more | GConflicting classifications of pathogenicity |
| | | Deletion (frameshift variant +1 more) | Arrhythmogenic right ventricular dysplasia 9 +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (nonsense) | not provided | |