| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC129994609, SHROOM1 (E197D) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129994609, SHROOM1 (G196R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129994609, SHROOM1 (E195D) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene