| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Duplication (intron variant) | Familial High Density Lipoprotein Deficiency +4 more | |
| | | Single nucleotide variant (intron variant) | not provided +2 more | |
| | | Single nucleotide variant (synonymous variant) | Hypoalphalipoproteinemia, primary, 1 +3 more | |
| | | Single nucleotide variant (intron variant) | not provided +3 more | |
| | | Duplication (intron variant) | not specified +4 more | |
Click to view in NCBI Gene