| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Monogenic diabetes +2 more | GConflicting classifications of pathogenicity |
| | | Indel (no sequence alteration) | Monogenic diabetes | |
| | | Single nucleotide variant (missense variant) | Congenital generalized lipodystrophy type 1 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | AGPAT2-related condition +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Monogenic diabetes +2 more | |
| | | Single nucleotide variant (missense variant) | Monogenic diabetes +1 more | |
| | | Single nucleotide variant (missense variant) | Monogenic diabetes +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Monogenic diabetes +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Monogenic diabetes | |
| | | Single nucleotide variant (missense variant) | Congenital generalized lipodystrophy type 1 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Monogenic diabetes | |
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