| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC130006119, MRPL11 (R25Q) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | LOC130006119, MRPL11 (R6P) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC130006119, MRPL11 (A7V) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC130006119, MRPL11 (M30V) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | LOC130006119, MRPL11 (G27S) | Single nucleotide variant (non-coding transcript variant +2 more) | Inborn genetic diseases | |
Click to view in NCBI Gene