| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (splice donor variant) | FXYD2-related disorder | |
| | | Single nucleotide variant (3 prime UTR variant) | FXYD2-related disorder | |
| | FXYD2, FXYD6-FXYD2 (G10S +3 more) | Single nucleotide variant (missense variant) | Renal hypomagnesemia 2 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | not provided +1 more | |
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