| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (synonymous variant) | DPAGT1-congenital disorder of glycosylation +2 more | |
| | | Single nucleotide variant (synonymous variant) | DPAGT1-congenital disorder of glycosylation +2 more | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | DPAGT1, LOC126861360 (P30S) | Single nucleotide variant (missense variant) | Congenital myasthenic syndrome 13 +2 more | GConflicting classifications of pathogenicity |
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