| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | DSCAM, LOC126653376 (V591L) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | DSCAM, LOC126653376 (T574M) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | DSCAM, LOC126653376 (Y532F) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | DSCAM, LOC126653376 (K511R) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
Click to view in NCBI Gene