| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC101928977, LOC129931253
+1 more (Q17E) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126805838, SLC22A15 (C519F) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC101928977, LOC129931253
+1 more (I15V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
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