| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC130056028, RGS6 (I226F +2 more) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | | Single nucleotide variant (synonymous variant +2 more) | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | See cases | |
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