| | TTN, TTN-AS1 (R32130fs +5 more) | Indel (frameshift variant) | Tibial muscular dystrophy | |
| | TTN, TTN-AS1 (E25514fs +5 more) | Deletion (frameshift variant) | Hypertrophic cardiomyopathy 9 +12 more | GConflicting classifications of pathogenicity |
| | LOC126806420, TTN +1 more (C33331R +5 more) | Single nucleotide variant (missense variant) | not provided +8 more | GConflicting classifications of pathogenicity |
| | TTN, TTN-AS1 (G23569S +5 more) | Single nucleotide variant (missense variant) | Cardiovascular phenotype +1 more | |
| | | Single nucleotide variant (intron variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +3 more | GConflicting classifications of pathogenicity |
| | LOC126806421, TTN +1 more (T29728I +5 more) | Single nucleotide variant (missense variant) | Tibial muscular dystrophy | |
| | TTN, TTN-AS1 (R29787S +5 more) | Single nucleotide variant (missense variant) | not provided +6 more | GConflicting classifications of pathogenicity |
| | TTN, TTN-AS1 (K28700T +5 more) | Single nucleotide variant (missense variant) | Tibial muscular dystrophy +9 more | GConflicting classifications of pathogenicity |
| | TTN, TTN-AS1 (I27407T +5 more) | Single nucleotide variant (missense variant) | not specified +7 more | GConflicting classifications of pathogenicity |
| | TTN, TTN-AS1 (E17660fs +5 more) | Deletion (frameshift variant) | Tibial muscular dystrophy | |
| | TTN, TTN-AS1 (S21967Y +5 more) | Single nucleotide variant (missense variant) | Cardiovascular phenotype +8 more | GConflicting classifications of pathogenicity |
| | TTN, TTN-AS1 (V20078M +5 more) | Single nucleotide variant (missense variant) | Cardiovascular phenotype +10 more | |
| | TTN-AS1, TTN (Y16889fs +5 more) | Duplication (frameshift variant) | Tibial muscular dystrophy | |
| | TTN, TTN-AS1 (R15054* +5 more) | Single nucleotide variant (nonsense) | Cardiomyopathy +5 more | GPathogenic/Likely pathogenic |
| | TTN, TTN-AS1 (G15988fs +5 more) | Deletion (frameshift variant) | Tibial muscular dystrophy +4 more | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1G +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | not specified +8 more | |
| | | Single nucleotide variant (missense variant +1 more) | Tibial muscular dystrophy +9 more | GConflicting classifications of pathogenicity |
| | | Deletion (intron variant) | Tibial muscular dystrophy +3 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 (missense variant +1 more) | Tibial muscular dystrophy | |
| | | Single nucleotide variant (intron variant) | Tibial muscular dystrophy | |
| | | Single nucleotide variant (missense variant +1 more) | Tibial muscular dystrophy | |
| | | Single nucleotide variant (missense variant +1 more) | Dilated cardiomyopathy 1G +6 more | GConflicting classifications of pathogenicity |
| | | Microsatellite (frameshift variant +1 more) | Tibial muscular dystrophy | |
| | LOC126806431, TTN (T5760fs +2 more) | Deletion (frameshift variant +1 more) | Tibial muscular dystrophy | |
| | | Single nucleotide variant (missense variant +1 more) | Tibial muscular dystrophy | |
| | | Single nucleotide variant (missense variant +1 more) | Right ventricular cardiomyopathy +1 more | |
| | | Single nucleotide variant (nonsense +1 more) | Hypertrophic cardiomyopathy 9 +8 more | |
| | LOC126806432, TTN (E4803K) | Single nucleotide variant (missense variant +1 more) | Tibial muscular dystrophy | |
| | | Single nucleotide variant (intron variant +1 more) | not specified +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Tibial muscular dystrophy | |
| | LOC101927055, TTN (R1330C +1 more) | Single nucleotide variant (missense variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +9 more | GConflicting classifications of pathogenicity |