| | | Copy number gain | not specified | |
| | | Single nucleotide variant (missense variant) | ACP4-related condition | |
| | | Microsatellite (inframe deletion) | ACP4-related condition | |
| | | Single nucleotide variant (synonymous variant) | ACP4-related condition | |
| | | Single nucleotide variant (missense variant) | ACP4-related condition | |
| | | Single nucleotide variant (intron variant) | ACP4-related condition | |
| | | Single nucleotide variant (synonymous variant) | ACP4-related condition | |
| | | Single nucleotide variant (synonymous variant) | ACP4-related condition | |
| | | Single nucleotide variant (synonymous variant) | ACP4-related condition | |
| | | Single nucleotide variant (synonymous variant) | ACP4-related condition | |
| | | Single nucleotide variant (splice donor variant) | ACP4-related condition | |
| | | Single nucleotide variant (synonymous variant) | ACP4-related condition | |
| | | Single nucleotide variant (intron variant) | ACP4-related condition | |
| | | Copy number gain | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ACP4, LOC130065005 (G314S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Amelogenesis imperfecta, type 1J | |
| | | Single nucleotide variant (missense variant) | Amelogenesis imperfecta, type 1J | |
| | | Single nucleotide variant (splice donor variant) | Amelogenesis imperfecta, type 1J | |
| | ACP4, LOC130065006 (A400D) | Single nucleotide variant (missense variant) | Amelogenesis imperfecta, type 1J | |
| | | Copy number gain | not provided | |
| | | Indel (frameshift variant) | not provided | |
| | | Single nucleotide variant (nonsense) | not provided | |
| | | Copy number gain | not specified | |
| | | Single nucleotide variant (missense variant) | Amelogenesis imperfecta | |
| | | Single nucleotide variant (missense variant) | Amelogenesis imperfecta | |
| | | Single nucleotide variant (missense variant) | Amelogenesis imperfecta | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (intron variant) | ACP4-related condition +1 more | |
| | | Copy number gain | not provided | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Single nucleotide variant (missense variant) | Amelogenesis imperfecta, type 1J | |
| | | Single nucleotide variant (missense variant) | Amelogenesis imperfecta, type 1J | |
| | | Single nucleotide variant (missense variant) | Amelogenesis imperfecta, type 1J | |
| | | Single nucleotide variant (missense variant) | Amelogenesis imperfecta, type 1J | |
| | | Single nucleotide variant (missense variant) | Amelogenesis imperfecta, type 1J | |
| | | Single nucleotide variant (missense variant) | Amelogenesis imperfecta, type 1J +1 more | |
| | | Single nucleotide variant (missense variant) | Amelogenesis imperfecta +1 more | GConflicting classifications of pathogenicity |
| | MIR498, MIR512-1 +782 more | Copy number gain | See cases | |
| | LOC113939975, LOC116286194 +806 more | Copy number gain | See cases | |
| | LOC130064933, LOC130064934 +1093 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC130065070, LOC130065071 +761 more | Copy number gain | See cases | |