| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC129936409, STT3B (D103Y) | Single nucleotide variant (missense variant) | STT3B-congenital disorder of glycosylation | |
| | | Single nucleotide variant (synonymous variant) | STT3B-congenital disorder of glycosylation | |
| | | Single nucleotide variant (intron variant) | STT3B-congenital disorder of glycosylation | |
Click to view in NCBI Gene