Links from MedGen
Items: 5
| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (synonymous variant +1 more) | Intellectual disability, autosomal dominant 33 +3 more | |
| | | Single nucleotide variant (intron variant +2 more) | Intellectual disability, autosomal dominant 33 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Ventricular fibrillation, paroxysmal familial, 2 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Ventricular fibrillation, paroxysmal familial, 2 +1 more | |
| | | Single nucleotide variant (intron variant) | not provided +1 more | |
Click to view in NCBI Gene