| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Cardiovascular phenotype +3 more | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Familial apolipoprotein C-II deficiency +3 more | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Cardiovascular phenotype +1 more | GPathogenic/Likely pathogenic |
Click to view in NCBI Gene