| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | CLDN7, LOC130060120 (T99A) | Single nucleotide variant (missense variant) | not specified | |
| | CLDN7, LOC130060120 (R106L) | Single nucleotide variant (missense variant) | not specified | |
| | CLDN7, LOC130060120 (M100T) | Single nucleotide variant (missense variant) | not specified | |
| | CLDN7, LOC130060120 (G109A) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
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