| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | DNAH17, LOC126862655 (V1405M) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | DNAH17, LOC126862655 (R1398H) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | DNAH17, LOC126862655 (E1394Q) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | DNAH17, LOC126862655 (T1380K) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
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