| | | Single nucleotide variant (missense variant) | Type 2 diabetes mellitus +5 more | |
| | | Single nucleotide variant (missense variant) | Monogenic diabetes | |
| | | Single nucleotide variant (missense variant) | not provided | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Diabetes mellitus | |
| | | Single nucleotide variant (missense variant) | Wolfram syndrome 1 +1 more | GUncertain significance/Uncertain risk allele |
| | | Single nucleotide variant (missense variant +1 more) | Type 1 diabetes mellitus 2 | |
| | | Single nucleotide variant (nonsense) | Cataract 41 +5 more | |
| | | Single nucleotide variant (missense variant) | Diabetes mellitus | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Diabetes mellitus | |
| | | Single nucleotide variant (missense variant) | Diabetes mellitus | |
| | | Single nucleotide variant (missense variant) | Maturity onset diabetes mellitus in young | |
| | | Deletion (frameshift variant +1 more) | Neonatal insulin-dependent diabetes mellitus | |
| | | Deletion (nonsense) | Wolfram syndrome 1 +1 more | |
| | | Single nucleotide variant (splice acceptor variant +1 more) | Maturity onset diabetes mellitus in young | |
| | | Deletion (frameshift variant) | Maturity onset diabetes mellitus in young | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Monogenic diabetes | |
| | | Single nucleotide variant (missense variant) | Monogenic diabetes | |
| | | Single nucleotide variant (missense variant) | Monogenic diabetes | |
| | | Deletion (splice donor variant +1 more) | Gastrointestinal stromal tumor +5 more | |
| | | Single nucleotide variant (nonsense) | Wolfram syndrome 1 +6 more | |
| | | Single nucleotide variant (missense variant) | Maturity-onset diabetes of the young type 7 +1 more | |
| | | Single nucleotide variant (missense variant) | WFS1-related condition +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | WFS1-related condition +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Diabetes mellitus +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +3 more | GPathogenic/Likely risk allele |
| | | Single nucleotide variant (missense variant) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Diabetes mellitus | |
| | | Single nucleotide variant (missense variant) | Permanent neonatal diabetes mellitus +8 more | |
| | | Single nucleotide variant (missense variant +1 more) | Type 2 diabetes mellitus +4 more | |
| | | Single nucleotide variant (missense variant) | Monogenic diabetes +9 more | |
| | | Single nucleotide variant (splice donor variant) | SPINK1-related condition +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | Monogenic diabetes +4 more | |
| | | Single nucleotide variant (missense variant) | not provided +11 more | |
| | | Single nucleotide variant (missense variant) | WFS1-related condition +4 more | |
| | | Single nucleotide variant (synonymous variant) | Diabetes mellitus +5 more | |
| | | Single nucleotide variant (nonsense +1 more) | Maturity-onset diabetes of the young type 2 +5 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Transitory neonatal diabetes mellitus +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Diabetes mellitus +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | PMM2-related condition +4 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (intron variant) | Hypoplastic pancreas-intestinal atresia-hypoplastic gallbalder syndrome +1 more | |