| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Cutis laxa, autosomal dominant 2 | |
| | | Single nucleotide variant (intron variant) | Cutis laxa, autosomal dominant 2 +1 more | GConflicting classifications of pathogenicity |
Click to view in NCBI Gene