| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant +1 more) | Autosomal dominant hyperinsulinism due to SUR1 deficiency +6 more | GPathogenic/Likely pathogenic |
| | | Microsatellite (frameshift variant +1 more) | Hyperinsulinemic hypoglycemia, familial, 1 +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (splice donor variant) | Transitory neonatal diabetes mellitus +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Hyperinsulinemic hypoglycemia, familial, 1 +9 more | GConflicting classifications of pathogenicity |
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