| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Single nucleotide variant (splice donor variant) | Hereditary pancreatitis +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Finnish congenital nephrotic syndrome +3 more | GConflicting classifications of pathogenicity; association; risk factor |
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