| | TTN, TTN-AS1 (I11405fs +5 more) | Microsatellite (frameshift variant) | Dilated cardiomyopathy 1G | |
| | TTN, TTN-AS1 (K14008fs +5 more) | Deletion (frameshift variant) | Dilated cardiomyopathy 1G | |
| | TTN, TTN-AS1 (I15761fs +5 more) | Duplication (frameshift variant) | Dilated cardiomyopathy 1G | |
| | TTN, TTN-AS1 (S25738* +5 more) | Single nucleotide variant (nonsense) | Dilated cardiomyopathy 1G | |
| | LOC126806422, TTN +1 more (E14274fs +5 more) | Deletion (frameshift variant) | Dilated cardiomyopathy 1G | |
| | | Single nucleotide variant (nonsense +1 more) | Dilated cardiomyopathy 1G | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Dilated cardiomyopathy 1G | |
| | TTN, TTN-AS1 (W10095G +5 more) | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1G | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1G | |
| | TTN, TTN-AS1 (W12248* +5 more) | Single nucleotide variant (nonsense) | Dilated cardiomyopathy 1G | |
| | | Duplication (frameshift variant) | Dilated cardiomyopathy 1G | |
| | | Indel (nonsense) | Dilated cardiomyopathy 1G | |
| | TTN, TTN-AS1 (A10029fs +5 more) | Deletion (frameshift variant) | Dilated cardiomyopathy 1G | |
| | TTN, TTN-AS1 (R17164* +5 more) | Single nucleotide variant (nonsense) | Dilated cardiomyopathy 1G | |
| | TTN, TTN-AS1 (G24104D +5 more) | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1G | |
| | TTN, TTN-AS1 (G11287R +5 more) | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1G | |
| | TTN, TTN-AS1 (K15637E +5 more) | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1G | |
| | LOC126806424, TTN +1 more (G10978* +5 more) | Single nucleotide variant (nonsense) | Dilated cardiomyopathy 1G | |
| | | Single nucleotide variant (missense variant +1 more) | Dilated cardiomyopathy 1G | |
| | | Single nucleotide variant (nonsense +1 more) | Dilated cardiomyopathy 1G | |
| | TTN, TTN-AS1 (R19120Q +5 more) | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1G | |
| | | Duplication (nonsense) | Dilated cardiomyopathy 1G | |
| | TTN, TTN-AS1 (E11083fs +5 more) | Duplication (non-coding transcript variant +1 more) | Dilated cardiomyopathy 1G | |
| | TTN, TTN-AS1 (L10004fs +5 more) | Deletion (frameshift variant) | Dilated cardiomyopathy 1G | |
| | TTN, TTN-AS1 (V17770fs +5 more) | Deletion (frameshift variant) | Dilated cardiomyopathy 1G | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (intron variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | TTN, TTN-AS1 (V7696fs +5 more) | Deletion (frameshift variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | LOC101927055, TTN (V1307fs +1 more) | Deletion (frameshift variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (intron variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (splice acceptor variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | TTN, TTN-AS1 (A32338fs +5 more) | Deletion (frameshift variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (intron variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (intron variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | TTN, TTN-AS1 (Y25090C +5 more) | Single nucleotide variant (missense variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | TTN, TTN-AS1 (E17874* +5 more) | Duplication (nonsense) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | TTN, TTN-AS1 (N22586fs +5 more) | Duplication (frameshift variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | TTN, TTN-AS1 (F6557fs +5 more) | Deletion (frameshift variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | TTN, TTN-AS1 (S14106fs +5 more) | Duplication (frameshift variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Deletion (frameshift variant +1 more) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | TTN, TTN-AS1 (M26487L +5 more) | Single nucleotide variant (missense variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (splice acceptor variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | TTN, TTN-AS1 (K18286* +5 more) | Single nucleotide variant (nonsense) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | LOC126806422, TTN +1 more (P14307fs +5 more) | Deletion (frameshift variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | TTN, TTN-AS1 (T14724fs +5 more) | Duplication (frameshift variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | TTN, TTN-AS1 (A20876fs +5 more) | Microsatellite (frameshift variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | TTN-AS1, LOC126806422 +1 more | Single nucleotide variant (synonymous variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (intron variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (splice donor variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (intron variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (splice donor variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | TTN, TTN-AS1 (K18145fs +5 more) | Microsatellite (frameshift variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | TTN, TTN-AS1 (W13428* +5 more) | Single nucleotide variant (nonsense) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (nonsense) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | TTN, TTN-AS1 (L14021fs +5 more) | Deletion (frameshift variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Deletion (splice donor variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | TTN, TTN-AS1 (P22733fs +5 more) | Duplication (frameshift variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (intron variant +1 more) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Deletion (frameshift variant +1 more) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Duplication (frameshift variant +1 more) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Duplication (frameshift variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | TTN, TTN-AS1 (K12542fs +5 more) | Duplication (frameshift variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | TTN, TTN-AS1 (R26689K +5 more) | Single nucleotide variant (missense variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Deletion (frameshift variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | TTN, TTN-AS1 (P13319fs +5 more) | Deletion (frameshift variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | TTN, TTN-AS1 (E6733* +5 more) | Single nucleotide variant (nonsense) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | TTN-AS1, TTN (T17723fs +5 more) | Deletion (frameshift variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Deletion (frameshift variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |