| | | 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) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | Alacrima, achalasia, and intellectual disability syndrome | |
| | | Single nucleotide variant (synonymous variant) | Alacrima, achalasia, and intellectual disability syndrome | |
| | | Single nucleotide variant (intron variant) | Alacrima, achalasia, and intellectual disability syndrome | |
| | | Deletion (frameshift variant) | Alacrima, achalasia, and intellectual disability syndrome | |
| | | Single nucleotide variant (intron variant) | Alacrima, achalasia, and intellectual disability syndrome | |
| | | Single nucleotide variant (intron variant) | Alacrima, achalasia, and intellectual disability syndrome | |
| | | Single nucleotide variant (splice donor variant) | not provided | |
| | | Single nucleotide variant (splice donor variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (nonsense) | GMPPA-related disorder | |
| | | Single nucleotide variant (nonsense) | Alacrima, achalasia, and intellectual disability syndrome +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | 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) | Alacrima, achalasia, and intellectual disability syndrome | |
| | | Single nucleotide variant (missense variant) | Alacrima, achalasia, and intellectual disability syndrome | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (synonymous variant) | Alacrima, achalasia, and intellectual disability syndrome | |
| | | 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 (intron variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (intron variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | Alacrima, achalasia, and intellectual disability syndrome | |
| | | Single nucleotide variant (missense variant) | Alacrima, achalasia, and intellectual disability syndrome | |
| | | Single nucleotide variant (missense variant) | Alacrima, achalasia, and intellectual disability syndrome | |
| | | Single nucleotide variant (synonymous variant) | Alacrima, achalasia, and intellectual disability syndrome | |
| | | Single nucleotide variant (missense variant) | Alacrima, achalasia, and intellectual disability syndrome | |
| | | Single nucleotide variant (synonymous variant) | Alacrima, achalasia, and intellectual disability syndrome | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (intron variant) | Alacrima, achalasia, and intellectual disability syndrome | |
| | | Single nucleotide variant (missense variant) | Alacrima, achalasia, and intellectual disability syndrome | |
| | | Single nucleotide variant (missense variant) | Alacrima, achalasia, and intellectual disability syndrome | |
| | | Single nucleotide variant (nonsense) | Alacrima, achalasia, and intellectual disability syndrome | |
| | | Single nucleotide variant (intron variant) | Alacrima, achalasia, and intellectual disability syndrome | |
| | | Single nucleotide variant (missense variant) | Alacrima, achalasia, and intellectual disability syndrome | |
| | | Duplication (frameshift variant) | not provided +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | Alacrima, achalasia, and intellectual disability syndrome | |
| | | Single nucleotide variant (synonymous variant) | Alacrima, achalasia, and intellectual disability syndrome | |
| | | Single nucleotide variant (intron variant) | Alacrima, achalasia, and intellectual disability syndrome | |
| | | Single nucleotide variant (synonymous variant) | Alacrima, achalasia, and intellectual disability syndrome | |
| | | Single nucleotide variant (synonymous variant) | Alacrima, achalasia, and intellectual disability syndrome | |
| | | Single nucleotide variant (intron variant) | Alacrima, achalasia, and intellectual disability syndrome | |
| | | Single nucleotide variant (missense variant) | Alacrima, achalasia, and intellectual disability syndrome | |
| | | Single nucleotide variant (synonymous variant) | Alacrima, achalasia, and intellectual disability syndrome | |
| | | Single nucleotide variant (missense variant) | Alacrima, achalasia, and intellectual disability syndrome | |
| | | Single nucleotide variant (missense variant) | Alacrima, achalasia, and intellectual disability syndrome | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (missense variant) | Alacrima, achalasia, and intellectual disability syndrome | |
| | | Single nucleotide variant (missense variant) | Alacrima, achalasia, and intellectual disability syndrome | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (nonsense) | Alacrima, achalasia, and intellectual disability syndrome | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | Alacrima, achalasia, and intellectual disability syndrome +1 more | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (nonsense) | Alacrima, achalasia, and intellectual disability syndrome | GPathogenic/Likely pathogenic |
| | | Deletion (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | Alacrima, achalasia, and intellectual disability syndrome | |
| | | Single nucleotide variant (synonymous variant) | Alacrima, achalasia, and intellectual disability syndrome | |
| | | Single nucleotide variant (missense variant) | Alacrima, achalasia, and intellectual disability syndrome | |
| | | Single nucleotide variant (missense variant) | Alacrima, achalasia, and intellectual disability syndrome | |
| | | Single nucleotide variant (missense variant) | Alacrima, achalasia, and intellectual disability syndrome | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | Alacrima, achalasia, and intellectual disability syndrome +2 more | |
| | | Single nucleotide variant (missense variant) | Alacrima, achalasia, and intellectual disability syndrome | |
| | | Single nucleotide variant (missense variant) | Alacrima, achalasia, and intellectual disability syndrome | |
| | | Single nucleotide variant (missense variant) | Alacrima, achalasia, and intellectual disability syndrome | |
| | | Single nucleotide variant (missense variant) | Alacrima, achalasia, and intellectual disability syndrome +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Alacrima, achalasia, and intellectual disability syndrome | |
| | | Deletion (intron variant) | Alacrima, achalasia, and intellectual disability syndrome | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | Alacrima, achalasia, and intellectual disability syndrome | |
| | | Single nucleotide variant (synonymous variant) | Alacrima, achalasia, and intellectual disability syndrome | |
| | | Single nucleotide variant (synonymous variant) | not provided | |