Gene entry
SFXN4
sideroflexin 4
- Chromosome
- 10
- Cytoband
- 10q26.11
- Variants (rsID)
- 10
SFXN4 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 10 (region 10q26.11). Its official name is “sideroflexin 4”. The reference table lists 10 variants (rsID) for this gene.
Clinically classified variants
2 reference-table entries with clinical significance.
- rs10749291Benignsingle nucleotide variantGrowth and developmental delay-hypotonia-vision impairment-lactic acidosis syndrome
- rs2275111Benignsingle nucleotide variantGrowth and developmental delay-hypotonia-vision impairment-lactic acidosis 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.