| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Copy number gain | See cases | |
| | LOC130064933, LOC130064934
+1093 more | Copy number gain | See cases | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | HRC, TRPM4 (A432T +3 more) | Single nucleotide variant (missense variant +1 more) | not provided +4 more | GConflicting classifications of pathogenicity |
| | HRC, TRPM4 (G582S +4 more) | Single nucleotide variant (missense variant) | Progressive familial heart block type IB +4 more | GConflicting classifications of pathogenicity |
Click to view in NCBI Gene