| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | KLHL18, LOC126806674 (A6V) | Single nucleotide variant (missense variant) | not specified | |
| | KLHL18, LOC126806674 (V13M) | Single nucleotide variant (missense variant) | not specified | |
| | KLHL18, LOC126806674 (P21S) | Single nucleotide variant (missense variant) | not specified | |
| | KLHL18, LOC126806674 (S22G) | Single nucleotide variant (missense variant) | not specified | |
| | KLHL18, LOC126806674 (D39N) | Single nucleotide variant (missense variant) | not specified | |
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