| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | EIF3B, LOC129997811 (A42S) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | EIF3B, LOC129997811 (T48S) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | EIF3B, LOC129997811 (A50T) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | EIF3B, LOC129997811 (R67S) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
Click to view in NCBI Gene