Gene entry
HAX1
HCLS1 associated protein X-1
- Chromosome
- 1
- Cytoband
- 1q21.3
- Variants (rsID)
- 3
HAX1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 1 (region 1q21.3). Its official name is “HCLS1 associated protein X-1”. The reference table lists 3 variants (rsID) for this gene.
Clinically classified variants
2 reference-table entries with clinical significance.
- rs146152769Conflicting interpretationssingle nucleotide variantKostmann syndrome
- rs138296453Uncertain significancesingle nucleotide variantKostmann syndrome
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.
