| | | Single nucleotide variant | GALT-related disorder +1 more | GConflicting classifications of pathogenicity |
| | | Indel (frameshift variant +1 more) | Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (intron variant) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | GALT-related disorder | |
| | | Single nucleotide variant (synonymous variant +1 more) | GALT-related disorder +1 more | GConflicting classifications of pathogenicity |
| | | Deletion (inframe_deletion +1 more) | not provided +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | GALT-related disorder +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (splice donor variant +1 more) | GALT-related disorder | |
| | | Single nucleotide variant (intron variant) | not specified +2 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (intron variant) | GALT-related disorder | |
| | | Deletion (intron variant) | Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | not specified +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not specified +1 more | |
| | | Single nucleotide variant (missense variant) | Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | GConflicting classifications of pathogenicity; other |
| | | Single nucleotide variant (synonymous variant) | not specified +1 more | |
| | | Single nucleotide variant (synonymous variant) | GALT-related disorder +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | GALT-related disorder | |