| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant +1 more) | Tay-Sachs disease +2 more | |
| | | Deletion (frameshift variant) | Tay-Sachs disease | |
| | | Single nucleotide variant (missense variant +1 more) | HEXA-related condition +4 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +1 more | GPathogenic/Likely pathogenic |
Click to view in NCBI Gene