| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (non-coding transcript variant +1 more) | SLAIN1-related disorder | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not specified | |
| | LOC130009927, SLAIN1 (S15P) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130009928, SLAIN1 (P172L) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130009928, SLAIN1 (K151R) | Single nucleotide variant (missense variant) | not specified | |
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