| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (intron variant) | Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency | |
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