Gene entry
NCF4
neutrophil cytosolic factor 4
- Chromosome
- 22
- Cytoband
- 22q12.3
- Variants (rsID)
- 14
NCF4 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 22 (region 22q12.3). Its official name is “neutrophil cytosolic factor 4”. The reference table lists 14 variants (rsID) for this gene.
Clinically classified variants
3 reference-table entries with clinical significance.
- rs2072712Benignsingle nucleotide variantGranulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 3
- rs56071149Benignsingle nucleotide variantGranulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 3
- rs143532979Conflicting interpretationssingle nucleotide variantGranulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 3
Other listed variants
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.