| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (synonymous variant) | not specified +5 more | |
| | KCNQ1, KCNQ1-AS1 (P631fs +1 more) | Deletion (frameshift variant) | KCNQ1-related condition +9 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (synonymous variant) | Cardiac arrhythmia +3 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Congenital long QT syndrome +5 more | |
Click to view in NCBI Gene