| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC124489741, LRRC55 (R152T) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC124489741, LRRC55 (H117Q) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene