| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +7 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy, familial restrictive, 1 +6 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (synonymous variant) | Hypertrophic cardiomyopathy +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (nonsense) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +9 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +8 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (intron variant) | Familial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant) | Familial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome +5 more | GConflicting classifications of pathogenicity |
| | DNAAF3, DNAAF3-AS1
+1 more | Single nucleotide variant (synonymous variant) | Familial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome +6 more | GConflicting classifications of pathogenicity |
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