| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | HCN4, LOC105370890
+1 more (R378C) | Single nucleotide variant (missense variant) | Sick sinus syndrome 2, autosomal dominant +4 more | GConflicting classifications of pathogenicity |
| | HCN4, LOC105370890
+1 more (R332Q) | Single nucleotide variant (missense variant) | not provided +2 more | |
Click to view in NCBI Gene