Links from MedGen
Items: 9
| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Neurodevelopmental disorder | |
| | | Single nucleotide variant (missense variant +1 more) | Neurodevelopmental disorder | |
| | | Single nucleotide variant (missense variant +1 more) | Neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities | |
| | | Single nucleotide variant (missense variant +1 more) | Neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities | |
| | | Indel (splice acceptor variant) | Neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities | |
| | | Single nucleotide variant (missense variant +1 more) | Neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities | |
| | | Single nucleotide variant (missense variant +1 more) | Neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities | |
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