| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC121587587, TMEM98 (V131M) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | TMEM98-related disorder | |
| | LOC121587587, TMEM98 (R134Q) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene