| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (intron variant) | not specified +2 more | |
| | | Single nucleotide variant (intron variant) | PGM1-congenital disorder of glycosylation +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | PGM1-congenital disorder of glycosylation +3 more | |
Click to view in NCBI Gene