| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant +1 more) | SLC35A2-congenital disorder of glycosylation +1 more | |
| | | Indel (splice donor variant +1 more) | SLC35A2-congenital disorder of glycosylation | |
| | | Single nucleotide variant (missense variant +2 more) | SLC35A2-congenital disorder of glycosylation | |
Click to view in NCBI Gene