| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | FASTKD2, LOC126806484 (R261C) | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | LOC126806484, FASTKD2 (M280V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FASTKD2, LOC126806484 (M280I) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
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