| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | SUDDEN INFANT DEATH SYNDROME +2 more | |
| | | Single nucleotide variant (missense variant) | Brugada syndrome +7 more | GConflicting classifications of pathogenicity |
| | | Deletion (splice donor variant +1 more) | SUDDEN INFANT DEATH SYNDROME +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Conduction disorder of the heart +6 more | |
| | | Single nucleotide variant (intron variant) | Brugada syndrome 1 +2 more | GConflicting classifications of pathogenicity |
Click to view in NCBI Gene