| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC101929319, TNFAIP6 (G90D) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC101929319, TNFAIP6 (R33L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC101929319, TNFAIP6 (R43L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | TNFAIP6, LOC101929319 (Y169H) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | TNFAIP6, LOC101929319 (L11V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
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