| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | HNRNPH2, RPL36A-HNRNPH2 (R206W) | Single nucleotide variant (3 prime UTR variant +1 more) | Neurodevelopmental disorder +6 more | GPathogenic/Likely pathogenic |
| | HNRNPH2, RPL36A-HNRNPH2 (R212S) | Single nucleotide variant (3 prime UTR variant +1 more) | not provided | |
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