| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC129992330, SEPSECS (I32V) | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | LOC129992330, SEPSECS (H28R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene