| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Homozygous familial hypercholesterolemia +9 more | GPathogenic/Likely pathogenic |
| | | Deletion (frameshift variant) | not provided +4 more | GPathogenic/Likely pathogenic |
Click to view in NCBI Gene