| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC126861190, TRAF6 (C20Y) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126861190, TRAF6 (N44S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene