| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC126806426, TTN +1 more (R16339W +5 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Cardiovascular phenotype +4 more | GConflicting classifications of pathogenicity |
| | LOC126806426, TTN +1 more (V13714I +5 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | GConflicting classifications of pathogenicity |
| | LOC126806426, TTN +1 more (R14587H +5 more) | Single nucleotide variant (missense variant) | Cardiovascular phenotype +4 more | GConflicting classifications of pathogenicity |
| | LOC126806426, TTN +1 more (K13655Q +5 more) | Single nucleotide variant (missense variant) | not provided | |
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