| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126861356, SCN4B (V152I +1 more) | Single nucleotide variant (missense variant +1 more) | Long QT syndrome 10 +2 more | |
| | LOC126861356, SCN4B (I116T +1 more) | Single nucleotide variant (missense variant +1 more) | Cardiovascular phenotype +2 more | |
Click to view in NCBI Gene