| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC130008440, PLXNC1 (P9L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130008440, PLXNC1 (P13T) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130008440, PLXNC1 (A17G) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene