| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | PPAN-P2RY11, LOC113939967
+1 more (A488D) | Single nucleotide variant (synonymous variant +1 more) | not provided +1 more | |
| | LOC113939967, P2RY11
+1 more (S507F) | Single nucleotide variant (synonymous variant +1 more) | PPAN-P2RY11-related disorder | |
| | LOC113939967, P2RY11
+1 more (S510Y) | Single nucleotide variant (synonymous variant +1 more) | P2RY11-related condition | |
| | LOC113939967, P2RY11
+1 more (A507T +1 more) | Single nucleotide variant (missense variant +1 more) | P2RY11-related condition | |
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