| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Deletion (3 prime UTR variant +1 more) | KRT86-related disorder +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | KRT81-related disorder | |
| | | Single nucleotide variant (missense variant +1 more) | not specified +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | KRT86-related disorder | |
| | | Single nucleotide variant (3 prime UTR variant) | KRT86-related disorder | |
Click to view in NCBI Gene