| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC114827827, NPPA
+1 more (P66L) | Single nucleotide variant (missense variant) | Atrial fibrillation, familial, 6 +2 more | |
| | LOC114827827, NPPA
+1 more (L43S) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | LOC114827827, NPPA
+1 more (N26K) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
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