| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | KRT3, LOC126861527 (E509K) | Single nucleotide variant (missense variant) | Corneal dystrophy, Meesmann, 2 | |
| | KRT3, LOC126861527 (R503P) | Single nucleotide variant (missense variant) | Corneal dystrophy, Meesmann, 2 | |
| | KRT3, LOC126861527 (E498V) | Single nucleotide variant (missense variant) | Corneal dystrophy, Meesmann, 2 | |
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