| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | PCDHG@, PCDHGA1
+20 more (S652I) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | PCDHGB7, PCDHGC3
+20 more (V698L) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | PCDHGA11, PCDHGA12
+21 more | Single nucleotide variant (synonymous variant) | not provided | |
| | | Copy number gain | not provided | |
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