| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (synonymous variant +1 more) | Cardiovascular phenotype +7 more | |
| | LOC126806426, TTN
+1 more (V14693M +5 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Hypertrophic cardiomyopathy +7 more | |
| | LOC126806426, TTN
+1 more (A13712T +5 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not provided +7 more | GConflicting classifications of pathogenicity |
| | LOC126806426, TTN
+1 more (D13683N +5 more) | Single nucleotide variant (missense variant) | not provided +6 more | |
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