Gene entry
NCF2
neutrophil cytosolic factor 2
- Chromosome
- 1
- Cytoband
- 1q25.3
- Variants (rsID)
- 17
NCF2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 1 (region 1q25.3). Its official name is “neutrophil cytosolic factor 2”. The reference table lists 17 variants (rsID) for this gene.
Clinically classified variants
9 reference-table entries with clinical significance.
- rs13306575Benignsingle nucleotide variantGranulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
- rs13306581Benignsingle nucleotide variantGranulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
- rs17849502Benignsingle nucleotide variantGranulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
- rs2274064Benignsingle nucleotide variantGranulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
- rs36113295Benignsingle nucleotide variantGranulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
- rs147744729Conflicting interpretationssingle nucleotide variantGranulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
- rs137878529Othersingle nucleotide variant
- rs267606912Othersingle nucleotide variantGranulomatous Disease, Chronic, Autosomal Recessive, 2
- rs119103274Pathogenicsingle nucleotide variantGranulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
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.