| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | TTN, TTN-AS1 (R23702fs +4 more) | Deletion (frameshift variant +1 more) | Cardiovascular phenotype +6 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Cardiovascular phenotype +6 more | GPathogenic/Likely pathogenic |
| | TTN, TTN-AS1 (E21509V +5 more) | Single nucleotide variant (missense variant) | not provided +1 more | |
| | TTN, TTN-AS1 (R19992Q +5 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not specified +3 more | |
| | | Single nucleotide variant (missense variant) | SUDDEN INFANT DEATH SYNDROME | |
Click to view in NCBI Gene