| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | HNRNPA2B1 (G311del +1 more) | Microsatellite (inframe_deletion) | not provided +1 more | |
| | | Single nucleotide variant (intron variant) | Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 2 | |
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