| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126859685, TNFRSF21 (P242R) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126859685, TNFRSF21 (R232C) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126859685, TNFRSF21 (K201T) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126859685, TNFRSF21 (R173W) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126859685, TNFRSF21 (R157W) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126859685, TNFRSF21 (V152L) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126859685, TNFRSF21 (V149A) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126859685, TNFRSF21 (V149M) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126859685, TNFRSF21 (A142S) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126859685, TNFRSF21 (M117V) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126859685, TNFRSF21 (I103V) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126859685, TNFRSF21 (P92T) | Single nucleotide variant (missense variant) | not specified | |
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