| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126806428, TTN (D7036N +2 more) | Single nucleotide variant (missense variant +1 more) | Cardiovascular phenotype +8 more | |
| | LOC126806428, TTN (A7015V +2 more) | Single nucleotide variant (missense variant +1 more) | Autosomal recessive limb-girdle muscular dystrophy type 2J +8 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Autosomal recessive limb-girdle muscular dystrophy type 2J +6 more | |
| | LOC126806428, TTN (A6954V +2 more) | Single nucleotide variant (missense variant +1 more) | Cardiovascular phenotype +7 more | |
Click to view in NCBI Gene