| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | HNRNPD, LOC129992757 (G49D) | Single nucleotide variant (missense variant) | not specified | |
| | HNRNPD, LOC129992757 (Q35fs) | Deletion (frameshift variant) | not provided | |
| | HNRNPD, LOC129992757 (A61V) | Single nucleotide variant (missense variant) | not specified | |
| | HNRNPD, LOC129992757 (S63A) | Single nucleotide variant (missense variant) | not specified | |
| | | Copy number loss | not provided | |
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