| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC130067862, SCO2
+1 more (L452fs +1 more) | Deletion (frameshift variant +1 more) | not specified +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +3 more) | not provided +2 more | |
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