| | LOC129996876, LOC129996877 +1449 more | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | LOC129389576, LOC129389577 +153 more | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | C6orf163, CFAP206 +16 more | Copy number loss | See cases | |
| | LOC129996783, ZNF292 (M1R) | Single nucleotide variant (5 prime UTR variant +2 more) | Intellectual developmental disorder, autosomal dominant 64 | |
| | LOC129996783, ZNF292 (E7K) | Single nucleotide variant (5 prime UTR variant +1 more) | ZNF292-related disorder | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | ZNF292-related disorder | |
| | LOC129996783, ZNF292 (G14S) | Single nucleotide variant (5 prime UTR variant +1 more) | Inborn genetic diseases | |
| | LOC129996783, ZNF292 (G16A) | Single nucleotide variant (5 prime UTR variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | not provided | |
| | LOC129996783, ZNF292 (A20T) | Single nucleotide variant (5 prime UTR variant +1 more) | Inborn genetic diseases | |
| | LOC129996783, ZNF292 (E21Q) | Single nucleotide variant (5 prime UTR variant +1 more) | Intellectual developmental disorder, autosomal dominant 64 | |
| | LOC129996783, ZNF292 (Q23P) | Single nucleotide variant (5 prime UTR variant +1 more) | not provided +1 more | |
| | LOC129996783, ZNF292 (E27Q) | Single nucleotide variant (5 prime UTR variant +1 more) | not provided | |
| | LOC129996783, ZNF292 (R28W) | Single nucleotide variant (5 prime UTR variant +1 more) | not provided | |
| | LOC129996783, ZNF292 (R40W) | Single nucleotide variant (5 prime UTR variant +1 more) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | ZNF292-related disorder | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | not provided | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Intellectual disability +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (splice donor variant) | Intellectual developmental disorder, autosomal dominant 64 | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | See cases | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Intellectual developmental disorder, autosomal dominant 64 | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | ZNF292-related disorder | |
| | | Deletion (frameshift variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Intellectual developmental disorder, autosomal dominant 64 | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (intron variant) | Intellectual developmental disorder, autosomal dominant 64 | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Intellectual developmental disorder, autosomal dominant 64 | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (nonsense) | Intellectual developmental disorder, autosomal dominant 64 | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Duplication (intron variant) | ZNF292-related disorder | |
| | | Deletion (intron variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (intron variant) | Intellectual developmental disorder, autosomal dominant 64 | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Deletion (frameshift variant) | Neurodevelopmental disorder | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Intellectual developmental disorder, autosomal dominant 64 +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Intellectual developmental disorder, autosomal dominant 64 | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Intellectual developmental disorder, autosomal dominant 64 | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (nonsense) | Intellectual developmental disorder, autosomal dominant 64 | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Intellectual developmental disorder, autosomal dominant 64 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (nonsense) | Intellectual developmental disorder, autosomal dominant 64 | |
| | | Single nucleotide variant (missense variant) | Intellectual developmental disorder, autosomal dominant 64 | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (nonsense) | Neurodevelopmental disorder | |
| | | Single nucleotide variant (missense variant) | Intellectual developmental disorder, autosomal dominant 64 | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | ZNF292-related disorder | |
| | | Single nucleotide variant (nonsense) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Deletion (frameshift variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Deletion (frameshift variant) | Intellectual developmental disorder, autosomal dominant 64 | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Deletion (frameshift variant) | Intellectual disability | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |