| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (synonymous variant) | Adult hypophosphatasia +5 more | |
| | | Single nucleotide variant (missense variant) | Childhood hypophosphatasia +6 more | |
| | | Deletion (intron variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +8 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | ALPL-related disorder +4 more | |
| | | Single nucleotide variant (missense variant) | Osteogenesis imperfecta +6 more | |
| | | Single nucleotide variant (intron variant) | not specified +4 more | |
| | | Single nucleotide variant (intron variant) | not specified +5 more | |
| | | Single nucleotide variant (intron variant) | not provided +5 more | |
| | | Single nucleotide variant (synonymous variant) | Hypophosphatasia +5 more | |
| | | Single nucleotide variant (intron variant) | Infantile hypophosphatasia +2 more | |
| | | Single nucleotide variant (missense variant) | Childhood hypophosphatasia +5 more | |
Click to view in NCBI Gene