| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126860190, WDR91 (T573M +3 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC126860190, WDR91 (R476H +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC126860190, WDR91 (A515T +3 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC126860190, WDR91 (D493G +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
Click to view in NCBI Gene