Gene entry
NHEJ1
non-homologous end joining factor 1
- Chromosome
- 2
- Cytoband
- 2q35
- Variants (rsID)
- 22
NHEJ1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 2 (region 2q35). Its official name is “non-homologous end joining factor 1”. The reference table lists 22 variants (rsID) for this gene.
Clinically classified variants
5 reference-table entries with clinical significance.
- rs34689457Benignsingle nucleotide variantCernunnos-XLF deficiency
- rs35270667Benignsingle nucleotide variantCernunnos-XLF deficiency
- rs118204451Conflicting interpretationssingle nucleotide variantCernunnos-XLF deficiency
- rs118204452Pathogenicsingle nucleotide variantCernunnos-XLF deficiency
- rs118204453Pathogenicsingle nucleotide variantCernunnos-XLF deficiency
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.