| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (intron variant) | Primary dilated cardiomyopathy +3 more | |
| | | Single nucleotide variant (synonymous variant) | Dilated cardiomyopathy 1G +2 more | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +2 more | |
| | LOC129935186, TTN
+1 more (K32393E +5 more) | Single nucleotide variant (missense variant) | Cardiovascular phenotype +1 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +2 more | |
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