| | | Single nucleotide variant (missense variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (intron variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (synonymous variant +1 more) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (synonymous variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (intron variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (synonymous variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (synonymous variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (synonymous variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (synonymous variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (synonymous variant) | PGM1-congenital disorder of glycosylation | |
| | | Deletion (intron variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (synonymous variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (synonymous variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (missense variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (synonymous variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (synonymous variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (intron variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (synonymous variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (synonymous variant) | PGM1-congenital disorder of glycosylation | |
| | | Duplication (frameshift variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (intron variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (intron variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (intron variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (synonymous variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (synonymous variant +1 more) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (missense variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (synonymous variant +1 more) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (synonymous variant) | PGM1-related disorder +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | PGM1-congenital disorder of glycosylation | |
| | | Indel (missense variant +1 more) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (intron variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (synonymous variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (synonymous variant +1 more) | PGM1-congenital disorder of glycosylation | |
| | | Deletion (frameshift variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (synonymous variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (synonymous variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (missense variant) | PGM1-congenital disorder of glycosylation | |
| | LOC129930668, PGM1 (F29fs) | Deletion (frameshift variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (missense variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (intron variant) | PGM1-congenital disorder of glycosylation | |
| | | Duplication | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (intron variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (synonymous variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (intron variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (missense variant) | PGM1-related disorder +1 more | |
| | | Indel (intron variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (synonymous variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (intron variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (missense variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (missense variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (intron variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (intron variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (intron variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (missense variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (synonymous variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (missense variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (missense variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (missense variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (synonymous variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (intron variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (missense variant +1 more) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (synonymous variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (synonymous variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (synonymous variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (synonymous variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (missense variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (intron variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (missense variant) | PGM1-congenital disorder of glycosylation +1 more | |
| | | Single nucleotide variant (synonymous variant) | PGM1-congenital disorder of glycosylation | |
| | LOC129930668, PGM1 (I40fs) | Deletion (frameshift variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (nonsense) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (synonymous variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (intron variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (intron variant) | PGM1-congenital disorder of glycosylation | |
| | | Indel (intron variant) | PGM1-congenital disorder of glycosylation | |
| | | Duplication (intron variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (intron variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (missense variant +1 more) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (synonymous variant +1 more) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (intron variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (synonymous variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (missense variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (missense variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (missense variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (missense variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (missense variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (intron variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (synonymous variant +1 more) | PGM1-congenital disorder of glycosylation +1 more | |
| | | Single nucleotide variant (missense variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (missense variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (synonymous variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (missense variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (missense variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (missense variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (synonymous variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (synonymous variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (intron variant) | PGM1-congenital disorder of glycosylation | |
| | | Single nucleotide variant (synonymous variant +1 more) | PGM1-congenital disorder of glycosylation +1 more | |
| | | Single nucleotide variant (missense variant) | PGM1-congenital disorder of glycosylation | |