| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC130066558, IFNAR2-IL10RB +1 more | Single nucleotide variant (intron variant) | IL10RB-related disorder +1 more | |
| | IFNAR2-IL10RB, IL10RB (E25K) | Single nucleotide variant (missense variant) | IL10RB-related disorder +1 more | |
| | IFNAR2-IL10RB, IL10RB (A44V) | Single nucleotide variant (missense variant) | IL10RB-related disorder +1 more | |
| | IFNAR2-IL10RB, IL10RB (V148M) | Single nucleotide variant (missense variant) | Inflammatory bowel disease 25 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Inflammatory bowel disease 25 +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | IL10RB-related disorder | |
| | IL10RB, IFNAR2-IL10RB (A243S) | Single nucleotide variant (missense variant) | IL10RB-related disorder +2 more | GConflicting classifications of pathogenicity |
| | IFNAR2-IL10RB, IL10RB (A255T) | Single nucleotide variant (missense variant) | IL10RB-related disorder +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Inflammatory bowel disease 25 +2 more | GConflicting classifications of pathogenicity |
Click to view in NCBI Gene