| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | CDC42BPB, LOC126862066 (R1243Q +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CDC42BPB, LOC126862066 (E1240Q +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CDC42BPB, LOC126862066 (L1262F +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene