| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | ANK2, LOC126807137 (G2293V +4 more) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | ANK2, LOC126807137 (S2655L +4 more) | Single nucleotide variant (missense variant +1 more) | not provided +2 more | GConflicting classifications of pathogenicity |
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