Gene entry
NFKBIA
NFKB inhibitor alpha
- Chromosome
- 14
- Cytoband
- 14q13.2
- Variants (rsID)
- 7
NFKBIA is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 14 (region 14q13.2). Its official name is “NFKB inhibitor alpha”. The reference table lists 7 variants (rsID) for this gene.
Clinically classified variants
5 reference-table entries with clinical significance.
- rs148656104Benignsingle nucleotide variantEctodermal dysplasia and immunodeficiency 2
- rs2273651Benignsingle nucleotide variantEctodermal dysplasia and immunodeficiency 2
- rs696Benignsingle nucleotide variantEctodermal dysplasia and immunodeficiency 2
- rs8904Benignsingle nucleotide variantEctodermal dysplasia and immunodeficiency 2
- rs142195196Conflicting interpretationssingle nucleotide variantEctodermal dysplasia and immunodeficiency 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.