| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC130007683, SLC2A13 (G57S) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130007683, SLC2A13 (A56V) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130007683, SLC2A13 (S53G) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130007683, SLC2A13 (S50I) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130007683, SLC2A13 (T49A) | Single nucleotide variant (missense variant) | not specified | |
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