| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | DSCC1, LOC130001014 (H27R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | DSCC1, LOC130001014 (E21Q) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene