| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | HNRNPA2B1 (G333fs +1 more) | Duplication | Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 2 +1 more | GConflicting classifications of pathogenicity |
| | HNRNPA2B1 (N323fs +1 more) | Deletion | Oculopharyngeal muscular dystrophy 2 | |
| | | Single nucleotide variant (synonymous variant) | not specified | |
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