| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC130064575, TMEM145 (E2K) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130064575, TMEM145 (G34S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130064575, TMEM145 (K39M) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene