| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Glycogen storage disease type X | |
| | DBNL, LOC129998342
+1 more (P123L) | Single nucleotide variant (3 prime UTR variant +1 more) | Glycogen storage disease type X +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | not provided +1 more | GConflicting classifications of pathogenicity |
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