| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC126862633, SLC39A11 (A146T) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | LOC126862633, SLC39A11 (E136K) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126862633, SLC39A11 (P130L) | Single nucleotide variant (missense variant) | not specified | |
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