| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (intron variant) | Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2 +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2 +2 more | |
Click to view in NCBI Gene