| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (5 prime UTR variant) | RPS27-related disorder | |
| | | Single nucleotide variant (intron variant) | RPS27-related disorder +1 more | |
| | LOC126805872, RPS27 (E13D) | Single nucleotide variant (missense variant +1 more) | RPS27-related disorder | |
| | LOC126805872, RPS27 (N29D) | Single nucleotide variant (missense variant +1 more) | RPS27-related disorder | |
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