| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC105370027, TMEM233 (M33T) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC105370027, TMEM233 (V43I) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC105370027, TMEM233 (Y4H) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC105370027, TMEM233 (N108K) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC105370027, TMEM233 (E29K) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene