| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | HES1, LOC129938190 (G157R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | HES1, LOC129938190 (A182T) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene