| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | MAP3K20, MAP3K20-AS1 (N222D) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | MAP3K20, MAP3K20-AS1 (R377Q) | Single nucleotide variant (missense variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | MAP3K20, MAP3K20-AS1 (E405G) | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | MAP3K20, MAP3K20-AS1 (R536K) | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
Click to view in NCBI Gene