| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC129993918, MAP3K1 (G28V) | Single nucleotide variant (missense variant) | not provided +1 more | |
| | LOC129993918, MAP3K1 (P153L) | Single nucleotide variant (missense variant) | not specified +2 more | GConflicting classifications of pathogenicity |
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