| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC130062628, TNFRSF11A (A5V) | Single nucleotide variant (missense variant) | Inborn genetic diseases +3 more | |
| | LOC130062628, TNFRSF11A (R6G) | Single nucleotide variant (missense variant) | not provided +1 more | |
Click to view in NCBI Gene