| | | Single nucleotide variant (missense variant) | SIN3A-related intellectual disability syndrome due to a point mutation | |
| | | Deletion (frameshift variant) | SIN3A-related intellectual disability syndrome due to a point mutation | |
| | | Duplication (frameshift variant) | SIN3A-related intellectual disability syndrome due to a point mutation | |
| | | Single nucleotide variant (missense variant) | SIN3A-related intellectual disability syndrome due to a point mutation | |
| | | Insertion (frameshift variant) | SIN3A-related intellectual disability syndrome due to a point mutation | |
| | | Single nucleotide variant (nonsense) | SIN3A-related intellectual disability syndrome due to a point mutation | |
| | | Single nucleotide variant (splice donor variant) | SIN3A-related intellectual disability syndrome due to a point mutation | |
| | | Single nucleotide variant (nonsense) | SIN3A-related intellectual disability syndrome due to a point mutation | |
| | | Single nucleotide variant (splice acceptor variant) | SIN3A-related intellectual disability syndrome due to a point mutation | |
| | | Duplication (splice acceptor variant) | SIN3A-related intellectual disability syndrome due to a point mutation | |
| | | Single nucleotide variant (nonsense) | not provided | |
| | | Duplication (nonsense) | SIN3A-related intellectual disability syndrome due to a point mutation | |
| | | Single nucleotide variant (nonsense) | SIN3A-related intellectual disability syndrome due to a point mutation | |
| | | Single nucleotide variant (missense variant) | SIN3A-related intellectual disability syndrome due to a point mutation | |
| | | Single nucleotide variant (missense variant) | SIN3A-related intellectual disability syndrome due to a point mutation | |
| | | Single nucleotide variant (missense variant) | SIN3A-related intellectual disability syndrome due to a point mutation | |
| | | Single nucleotide variant (missense variant) | SIN3A-related intellectual disability syndrome due to a point mutation | |
| | | Single nucleotide variant (synonymous variant) | SIN3A-related intellectual disability syndrome due to a point mutation | |
| | | Single nucleotide variant (missense variant) | SIN3A-related intellectual disability syndrome due to a point mutation | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (nonsense) | SIN3A-related intellectual disability syndrome due to a point mutation +2 more | |
| | | Single nucleotide variant (intron variant) | SIN3A-related intellectual disability syndrome due to a point mutation | |
| | | Deletion (frameshift variant) | SIN3A-related intellectual disability syndrome due to a point mutation | |
| | | Single nucleotide variant (missense variant) | SIN3A-related intellectual disability syndrome due to a point mutation | |
| | | Single nucleotide variant (missense variant) | SIN3A-related intellectual disability syndrome due to a point mutation | |
| | | Deletion (frameshift variant) | SIN3A-related intellectual disability syndrome due to a point mutation | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (nonsense) | SIN3A-related intellectual disability syndrome due to a point mutation | |
| | | Single nucleotide variant (missense variant) | SIN3A-related intellectual disability syndrome due to a point mutation | |
| | | Duplication (frameshift variant) | SIN3A-related intellectual disability syndrome due to a point mutation | |
| | | Single nucleotide variant (synonymous variant) | SIN3A-related intellectual disability syndrome due to a point mutation | |
| | | Single nucleotide variant (missense variant) | SIN3A-related intellectual disability syndrome due to a point mutation | |
| | | Single nucleotide variant (missense variant) | SIN3A-related intellectual disability syndrome due to a point mutation | |
| | | Duplication (frameshift variant) | SIN3A-related intellectual disability syndrome due to a point mutation | |
| | | Microsatellite (frameshift variant) | SIN3A-related intellectual disability syndrome due to a point mutation | |
| | | Single nucleotide variant (intron variant) | SIN3A-related intellectual disability syndrome due to a point mutation +1 more | |
| | | Single nucleotide variant (nonsense) | SIN3A-related intellectual disability syndrome due to a point mutation +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | SIN3A-related intellectual disability syndrome due to a point mutation | |
| | | Single nucleotide variant (nonsense) | SIN3A-related intellectual disability syndrome due to a point mutation | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | SIN3A-related intellectual disability syndrome due to a point mutation | |
| | | Duplication (frameshift variant) | SIN3A-related intellectual disability syndrome due to a point mutation | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | SIN3A-related intellectual disability syndrome due to a point mutation | |
| | | Single nucleotide variant (intron variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | SIN3A-related intellectual disability syndrome due to a point mutation | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | SIN3A-related intellectual disability syndrome due to a point mutation | |
| | | Single nucleotide variant (nonsense) | SIN3A-related intellectual disability syndrome due to a point mutation | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | SIN3A-related intellectual disability syndrome due to a point mutation | |
| | | Duplication (frameshift variant) | SIN3A-related intellectual disability syndrome due to a point mutation | |
| | | Single nucleotide variant (missense variant) | SIN3A-related intellectual disability syndrome due to a point mutation | |
| | | Deletion (frameshift variant) | SIN3A-related intellectual disability syndrome due to a point mutation | |
| | | Single nucleotide variant (nonsense) | SIN3A-related intellectual disability syndrome due to a point mutation | |
| | | Single nucleotide variant (missense variant) | SIN3A-related intellectual disability syndrome due to a point mutation | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Duplication (frameshift variant) | SIN3A-related intellectual disability syndrome due to a point mutation | |
| | | Duplication | SIN3A-related intellectual disability syndrome due to a point mutation | |
| | | Deletion (frameshift variant) | not provided +1 more | GPathogenic/Likely pathogenic |
| | | Deletion (frameshift variant) | not provided | |
| | | Microsatellite (frameshift variant) | SIN3A-related intellectual disability syndrome due to a point mutation | |
| | | Single nucleotide variant (nonsense) | SIN3A-related intellectual disability syndrome due to a point mutation | |
| | | Microsatellite (frameshift variant) | SIN3A-related intellectual disability syndrome due to a point mutation | |
| | | Deletion (frameshift variant) | SIN3A-related intellectual disability syndrome due to a point mutation | |
| | | Deletion | SIN3A-related intellectual disability syndrome due to a point mutation | |
| | | Duplication (frameshift variant) | SIN3A-related intellectual disability syndrome due to a point mutation | |