| | LOC101927055, TTN (T1580M +1 more) | Single nucleotide variant (missense variant +1 more) | not specified +8 more | |
| | LOC101927055, TTN (R1572Q +1 more) | Single nucleotide variant (missense variant +1 more) | Cardiovascular phenotype +6 more | |
| | | Single nucleotide variant (intron variant +1 more) | not specified +5 more | |
| | LOC101927055, TTN (I1544V +1 more) | Single nucleotide variant (missense variant +1 more) | not provided +8 more | |
| | | Single nucleotide variant (intron variant +1 more) | Autosomal recessive limb-girdle muscular dystrophy type 2J +6 more | |
| | LOC101927055, TTN (F1466L +1 more) | Single nucleotide variant (missense variant +1 more) | Autosomal recessive limb-girdle muscular dystrophy type 2J +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Dilated cardiomyopathy 1G +8 more | |
| | LOC101927055, TTN (R1441P +1 more) | Single nucleotide variant (missense variant +1 more) | Dilated cardiomyopathy 1G +8 more | |
| | LOC101927055, TTN (R1416C +1 more) | Single nucleotide variant (missense variant +1 more) | Autosomal recessive limb-girdle muscular dystrophy type 2J +9 more | |
| | LOC101927055, TTN (S1400T +1 more) | Single nucleotide variant (missense variant) | not specified +8 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) | Dilated cardiomyopathy 1G +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not specified +8 more | |
| | LOC101927055, TTN (R1330C +1 more) | Single nucleotide variant (missense variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | LOC101927055, TTN (S1295L +1 more) | Single nucleotide variant (missense variant) | Tibial muscular dystrophy +7 more | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +6 more | |