| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126806895, MAP3K13 (I632T +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126806895, MAP3K13 (D658G +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126806895, MAP3K13 (R673C +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126806895, MAP3K13 (E883K +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126806895, MAP3K13 (R915C +1 more) | Single nucleotide variant (missense variant) | not specified | |
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