| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not specified +5 more | |
| | | Single nucleotide variant (missense variant) | X-linked distal spinal muscular atrophy type 3 +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | X-linked distal spinal muscular atrophy type 3 +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | |
| | | Single nucleotide variant (missense variant) | Menkes kinky-hair syndrome +2 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Menkes kinky-hair syndrome +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | not specified +5 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Ehlers-Danlos syndrome +5 more | |
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