| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | DNAH9, LOC126862506 (V1625I) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | DNAH9, LOC126862506 (S1646R) | Single nucleotide variant (missense variant) | not provided +1 more | |
| | DNAH9, LOC126862506 (T1652R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
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