| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC129935184, TTN
+1 more (I32620L +5 more) | Single nucleotide variant (missense variant) | not specified +1 more | |
| | LOC129935184, TTN
+1 more (T35185I +5 more) | Single nucleotide variant (missense variant) | not provided +2 more | |
| | LOC129935184, TTN
+1 more (Y32614H +5 more) | Single nucleotide variant (missense variant) | not provided | |
| | LOC129935184, TTN
+1 more (R32606H +5 more) | Single nucleotide variant (missense variant) | Cardiovascular phenotype +4 more | |
| | LOC129935184, TTN
+1 more (S35172del +5 more) | Deletion (inframe_deletion) | Cardiomyopathy +8 more | GConflicting classifications of pathogenicity |
Click to view in NCBI Gene