| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC126806427, TTN (D12499N +5 more) | Single nucleotide variant (missense variant) | not specified +7 more | |
| | LOC126806427, TTN (S15043N +5 more) | Single nucleotide variant (missense variant) | Cardiovascular phenotype +7 more | |
| | LOC126806427, TTN (N12433H +5 more) | Single nucleotide variant (missense variant) | not specified +7 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +7 more | GConflicting classifications of pathogenicity |
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