| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | KRT5, LOC126861525 (A408T) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | KRT5, LOC126861525 (Q406K) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | KRT5, LOC126861525 (R391W) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | KRT5, LOC126861525 (H375R) | Single nucleotide variant (missense variant) | not provided +1 more | |
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