| | | Single nucleotide variant (non-coding transcript variant +1 more) | TTN-related disorder | |
| | LOC101927055, TTN (R1572Q +1 more) | Single nucleotide variant (missense variant +1 more) | Cardiovascular phenotype +6 more | |
| | LOC101927055, TTN (I1567T +1 more) | Single nucleotide variant (missense variant +1 more) | Dilated cardiomyopathy 1G +7 more | |
| | LOC101927055, TTN (M1557I +1 more) | Single nucleotide variant (missense variant +1 more) | TTN-related disorder +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant +1 more) | Autosomal recessive limb-girdle muscular dystrophy type 2J +6 more | |
| | LOC101927055, TTN (R1453S +1 more) | Single nucleotide variant (missense variant +1 more) | Autosomal recessive limb-girdle muscular dystrophy type 2J +7 more | GConflicting classifications of pathogenicity |
| | LOC101927055, TTN (R1416H +1 more) | Single nucleotide variant (missense variant +1 more) | TTN-related disorder +1 more | GConflicting classifications of pathogenicity |
| | LOC101927055, TTN (I1393V +1 more) | Single nucleotide variant (missense variant) | Cardiovascular phenotype +7 more | |
| | LOC101927055, TTN (G1345D +1 more) | Single nucleotide variant (missense variant) | Tibial muscular dystrophy +8 more | GConflicting classifications of pathogenicity |
| | LOC101927055, TTN (L1273I +1 more) | Single nucleotide variant (missense variant) | TTN-related disorder | |
| | LOC101927055, TTN (S1295L +1 more) | Single nucleotide variant (missense variant) | not specified +7 more | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +6 more | |