| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (intron variant) | not specified +6 more | GConflicting classifications of pathogenicity |
| | CFTR, LOC111674472 (L997F) | Single nucleotide variant (missense variant) | not specified +5 more | GConflicting classifications of pathogenicity |
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