| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC130010096, TNFSF13B (T62A) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130010096, TNFSF13B (T51S) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130010096, TNFSF13B (V69M) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130010096, TNFSF13B (L48Q) | Single nucleotide variant (missense variant) | not specified | |
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