| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | RPL36A-HNRNPH2, HNRNPH2 (R206W) | Single nucleotide variant (3 prime UTR variant +1 more) | Inborn genetic diseases +6 more | GPathogenic/Likely pathogenic |
| | HNRNPH2, RPL36A-HNRNPH2 (Y210C) | Single nucleotide variant (3 prime UTR variant +1 more) | Intellectual disability, X-linked, syndromic, Bain type +2 more | GConflicting classifications of pathogenicity |
Click to view in NCBI Gene