| | TTN, TTN-AS1 (S35972I +5 more) | Single nucleotide variant (missense variant) | Cardiovascular phenotype +2 more | GConflicting classifications of pathogenicity |
| | TTN, TTN-AS1 (C35918Y +5 more) | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1G +5 more | GConflicting classifications of pathogenicity |
| | TTN, TTN-AS1 (T26850K +5 more) | Single nucleotide variant (missense variant) | not provided | |
| | TTN, TTN-AS1 (P26831L +5 more) | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1G +2 more | |
| | TTN, TTN-AS1 (G33323S +5 more) | Single nucleotide variant (missense variant) | not provided +4 more | GConflicting classifications of pathogenicity |
| | TTN-AS1, TTN (S34198R +5 more) | Single nucleotide variant (missense variant) | Cardiovascular phenotype +3 more | GConflicting classifications of pathogenicity |
| | TTN, TTN-AS1 (E35796A +5 more) | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1G +2 more | GConflicting classifications of pathogenicity |
| | TTN, TTN-AS1 (V33227A +5 more) | Single nucleotide variant (missense variant) | not provided | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (splice donor variant) | Cardiovascular phenotype +9 more | GConflicting classifications of pathogenicity |
| | TTN, TTN-AS1 (I35664V +5 more) | Single nucleotide variant (missense variant) | not provided +3 more | |
| | TTN, TTN-AS1 (R35652Q +5 more) | Single nucleotide variant (missense variant) | Cardiovascular phenotype +8 more | GConflicting classifications of pathogenicity |
| | TTN, TTN-AS1 (W33997C +5 more) | Single nucleotide variant (missense variant) | not provided +3 more | |
| | TTN, TTN-AS1 (A26534P +5 more) | Single nucleotide variant (missense variant) | Cardiovascular phenotype +1 more | GConflicting classifications of pathogenicity |
| | TTN, TTN-AS1 (E26526K +5 more) | Single nucleotide variant (missense variant) | not provided +2 more | |
| | TTN, TTN-AS1 (E32991Q +5 more) | Single nucleotide variant (missense variant) | not specified +10 more | GConflicting classifications of pathogenicity |
| | TTN, TTN-AS1 (K26393E +5 more) | Single nucleotide variant (missense variant) | not provided | |
| | LOC129935183, TTN
+1 more (V35253M +5 more) | Single nucleotide variant (missense variant) | not provided +6 more | GConflicting classifications of pathogenicity |
| | LOC129935183, TTN
+1 more (A32678G +5 more) | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1G +3 more | GConflicting classifications of pathogenicity |
| | LOC129935183, TTN
+1 more (V35203A +5 more) | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1G +2 more | GConflicting classifications of pathogenicity |
| | LOC129935184, TTN
+1 more (I32620L +5 more) | Single nucleotide variant (missense variant) | not specified +1 more | |
| | LOC129935184, TTN
+1 more (S35172del +5 more) | Deletion (inframe_deletion) | Cardiomyopathy +8 more | GConflicting classifications of pathogenicity |
| | TTN, TTN-AS1 (E26077K +5 more) | Single nucleotide variant (missense variant) | not specified +2 more | GConflicting classifications of pathogenicity |
| | LOC129935185, TTN
+1 more (D35045V +5 more) | Single nucleotide variant (missense variant) | not specified +3 more | |
| | TTN, TTN-AS1 (E34984D +5 more) | Single nucleotide variant (missense variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +3 more | |
| | TTN, TTN-AS1 (S25885L +5 more) | Single nucleotide variant (missense variant) | not provided +2 more | |
| | TTN, TTN-AS1 (P34887L +5 more) | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1G +6 more | |
| | TTN, TTN-AS1 (E33228K +5 more) | Single nucleotide variant (missense variant) | not provided +4 more | GConflicting classifications of pathogenicity |
| | TTN, TTN-AS1 (R34861H +5 more) | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1G +7 more | |
| | TTN, TTN-AS1 (R32273H +5 more) | Single nucleotide variant (missense variant) | Cardiovascular phenotype +8 more | GConflicting classifications of pathogenicity |
| | TTN, TTN-AS1 (R33164Q +5 more) | Single nucleotide variant (missense variant) | not specified +4 more | GConflicting classifications of pathogenicity |
| | TTN, TTN-AS1 (R25735fs +5 more) | Deletion (frameshift variant) | Primary dilated cardiomyopathy +5 more | GConflicting classifications of pathogenicity |
| | TTN, TTN-AS1 (D25660A +5 more) | Single nucleotide variant (missense variant) | not provided +2 more | |
| | TTN, TTN-AS1 (E32109D +5 more) | Single nucleotide variant (missense variant) | not provided +2 more | |
| | TTN, TTN-AS1 (R25531C +5 more) | Single nucleotide variant (missense variant) | not provided +2 more | |
| | TTN, TTN-AS1 (R32007C +5 more) | Single nucleotide variant (missense variant) | not provided | |
| | TTN, TTN-AS1 (V34563A +5 more) | Single nucleotide variant (missense variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +9 more | GConflicting classifications of pathogenicity |
| | TTN, TTN-AS1 (V34563M +5 more) | Single nucleotide variant (missense variant) | not provided +3 more | |
| | TTN, TTN-AS1 (I31985T +5 more) | Single nucleotide variant (missense variant) | not provided +4 more | GConflicting classifications of pathogenicity |
| | TTN, TTN-AS1 (K25658E +5 more) | Single nucleotide variant (missense variant) | Cardiovascular phenotype +1 more | |
| | TTN, TTN-AS1 (V34473I +4 more) | Single nucleotide variant (missense variant) | not specified +7 more | GConflicting classifications of pathogenicity |
| | TTN, TTN-AS1 (E25514fs +5 more) | Deletion (frameshift variant) | Cardiovascular phenotype +12 more | GConflicting classifications of pathogenicity |
| | TTN, TTN-AS1 (T34431M +5 more) | Single nucleotide variant (missense variant) | Tibial muscular dystrophy +8 more | GConflicting classifications of pathogenicity |
| | TTN-AS1, TTN (M34251K +5 more) | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1G +2 more | |
| | TTN, TTN-AS1 (M31683V +5 more) | Single nucleotide variant (missense variant) | not specified +9 more | GConflicting classifications of pathogenicity |
| | TTN, TTN-AS1 (C25144Y +5 more) | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1G +2 more | |
| | TTN, TTN-AS1 (A25080T +5 more) | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1G +2 more | |
| | TTN, TTN-AS1 (I34133T +5 more) | Single nucleotide variant (missense variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +3 more | |
| | TTN, TTN-AS1 (R34110P +5 more) | Single nucleotide variant (missense variant) | not provided +2 more | |
| | TTN, TTN-AS1 (Q25004R +5 more) | Single nucleotide variant (missense variant) | Cardiovascular phenotype +1 more | |
| | TTN, TTN-AS1 (A34064T +5 more) | Single nucleotide variant (missense variant) | Tibial muscular dystrophy +7 more | GConflicting classifications of pathogenicity |
| | TTN, TTN-AS1 (R34061H +5 more) | Single nucleotide variant (missense variant) | Cardiovascular phenotype +3 more | |
| | TTN, TTN-AS1 (E34041K +5 more) | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1G +6 more | |
| | TTN-AS1, TTN (L34009F +5 more) | Single nucleotide variant (missense variant) | not provided +2 more | |
| | TTN, TTN-AS1 (R33964S +5 more) | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1G +7 more | GConflicting classifications of pathogenicity |
| | TTN, TTN-AS1 (R31373T +5 more) | Single nucleotide variant (missense variant) | not provided +3 more | |
| | TTN, TTN-AS1 (Q25055R +5 more) | Single nucleotide variant (missense variant) | not provided +1 more | |
| | TTN, TTN-AS1 (K24778N +5 more) | Single nucleotide variant (missense variant) | Myopathy, myofibrillar, 9, with early respiratory failure +6 more | |
| | TTN-AS1, TTN (R31193W +5 more) | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1G +9 more | GConflicting classifications of pathogenicity |
| | TTN, TTN-AS1 (R24638Q +5 more) | Single nucleotide variant (missense variant) | not provided +3 more | GConflicting classifications of pathogenicity |
| | TTN, TTN-AS1 (R24596G +5 more) | Single nucleotide variant (missense variant) | not provided | |
| | TTN, TTN-AS1 (G33550D +5 more) | Single nucleotide variant (missense variant) | not provided +3 more | |
| | TTN, TTN-AS1 (F24483L +5 more) | Single nucleotide variant (missense variant) | Cardiovascular phenotype +1 more | GConflicting classifications of pathogenicity |
| | TTN, TTN-AS1 (N24441K +5 more) | Single nucleotide variant (missense variant) | not provided | |
| | TTN, TTN-AS1 (G33473S +5 more) | Single nucleotide variant (missense variant) | not provided +8 more | GConflicting classifications of pathogenicity |
| | TTN, TTN-AS1 (C24404W +5 more) | Single nucleotide variant (missense variant) | not provided | |
| | TTN, TTN-AS1 (V30899G +5 more) | Single nucleotide variant (missense variant) | Cardiovascular phenotype +9 more | GConflicting classifications of pathogenicity |
| | LOC126806420, TTN
+1 more (R30864H +5 more) | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1G +3 more | GConflicting classifications of pathogenicity |
| | LOC126806420, TTN
+1 more (C33331R +5 more) | Single nucleotide variant (missense variant) | Tibial muscular dystrophy +8 more | GConflicting classifications of pathogenicity |
| | LOC126806420, TTN
+1 more (W33322C +5 more) | Single nucleotide variant (missense variant) | Tibial muscular dystrophy +7 more | GConflicting classifications of pathogenicity |
| | LOC126806420, TTN
+1 more (E33301K +5 more) | Single nucleotide variant (missense variant) | Cardiovascular phenotype +9 more | GConflicting classifications of pathogenicity |
| | TTN, TTN-AS1 (R30536C +5 more) | Single nucleotide variant (missense variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +7 more | GConflicting classifications of pathogenicity |
| | TTN, TTN-AS1 (S23922L +5 more) | Indel (non-coding transcript variant +1 more) | Dilated cardiomyopathy 1G +8 more | GConflicting classifications of pathogenicity |
| | TTN, TTN-AS1 (S23852F +5 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Cardiovascular phenotype +1 more | GConflicting classifications of pathogenicity |
| | TTN, TTN-AS1 (S30347G +5 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Cardiomyopathy +6 more | GConflicting classifications of pathogenicity |
| | TTN, TTN-AS1 (P23839del +5 more) | Microsatellite (non-coding transcript variant) | not provided | |
| | TTN, TTN-AS1 (A30274T +5 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not specified +3 more | |
| | TTN-AS1, TTN (D30254G +5 more) | Single nucleotide variant (missense variant +1 more) | not specified +6 more | GConflicting classifications of pathogenicity |
| | TTN, TTN-AS1 (D32822N +5 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not provided +2 more | |
| | TTN, TTN-AS1 (G29959S +5 more) | Single nucleotide variant (missense variant) | Cardiomyopathy +2 more | GConflicting classifications of pathogenicity |
| | TTN, TTN-AS1 (R29926H +5 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Cardiovascular phenotype +7 more | GConflicting classifications of pathogenicity |
| | TTN, TTN-AS1 (I30841T +5 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not specified +1 more | |
| | TTN, TTN-AS1 (R23408C +5 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Autosomal recessive limb-girdle muscular dystrophy type 2J +3 more | |
| | TTN, TTN-AS1 (R29876H +5 more) | Single nucleotide variant (missense variant) | Cardiomyopathy +2 more | |
| | TTN, TTN-AS1 (V23372L +5 more) | Single nucleotide variant (missense variant) | not provided | |
| | TTN, TTN-AS1 (I23342T +5 more) | Single nucleotide variant (missense variant) | not provided | |
| | TTN, TTN-AS1 (P29832T +5 more) | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1G +7 more | GConflicting classifications of pathogenicity |
| | TTN, TTN-AS1 (R32367C +5 more) | Single nucleotide variant (missense variant) | not specified +8 more | GConflicting classifications of pathogenicity |
| | TTN, TTN-AS1 (E29783K +5 more) | Single nucleotide variant (missense variant) | not specified +7 more | |
| | TTN-AS1, TTN (I32330T +4 more) | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1G +8 more | GConflicting classifications of pathogenicity |
| | LOC126806421, TTN
+1 more (P23247S +5 more) | Single nucleotide variant (missense variant) | Cardiovascular phenotype +7 more | |
| | LOC126806421, TTN
+1 more (W32249R +4 more) | Single nucleotide variant (missense variant) | not provided | |
| | LOC126806421, TTN
+1 more (D30572N +5 more) | Single nucleotide variant (missense variant) | Cardiovascular phenotype +7 more | GConflicting classifications of pathogenicity |
| | LOC126806421, TTN
+1 more (R23205H +5 more) | Single nucleotide variant (missense variant) | not provided +6 more | |
| | LOC126806421, TTN
+1 more (E23078G +5 more) | Single nucleotide variant (missense variant) | not provided | |
| | LOC126806421, TTN
+1 more (R29490W +5 more) | Single nucleotide variant (missense variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | LOC126806421, TTN
+1 more (I32053M +5 more) | Single nucleotide variant (missense variant) | not provided | |
| | LOC126806421, TTN
+1 more (D29450E +5 more) | Single nucleotide variant (missense variant) | not provided | |
| | TTN, TTN-AS1 (S22932G +5 more) | Single nucleotide variant (missense variant) | not provided | |
| | TTN, TTN-AS1 (N30321D +5 more) | Single nucleotide variant (missense variant) | Cardiovascular phenotype +2 more | GConflicting classifications of pathogenicity |
| | TTN-AS1, TTN (P31906A +5 more) | Single nucleotide variant (missense variant) | not provided +2 more | |