| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC112694701, TTLL9 (E148K) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | LOC112694701, TTLL9 (R121W) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | LOC112694701, TTLL9 (R109Q) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
Click to view in NCBI Gene