| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126862785, RTTN (K1836R +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | LOC126862785, RTTN (N1834D +1 more) | Single nucleotide variant (missense variant) | not provided +1 more | |
| | LOC126862785, RTTN (V1824M +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126862785, RTTN (F1777S +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene