| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC130006069, SNX32 (G180E) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130006069, SNX32 (T195M) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130006069, SNX32 (G196D) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130006069, SNX32 (M197T) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130006069, SNX32 (L200I) | Single nucleotide variant (missense variant) | not specified | |
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