| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC130063326, TNFSF14 (L45S) | Single nucleotide variant (intron variant +1 more) | Inborn genetic diseases | |
| | LOC130063326, TNFSF14 (Q31R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene