Gene entry
ARSH
arylsulfatase family member H
- Chromosome
- X
- Cytoband
- Xp22.33
- Variants (rsID)
- 12
ARSH is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome X (region Xp22.33). Its official name is “arylsulfatase family member H”. The reference table lists 12 variants (rsID) for this gene.
Clinically classified variants
2 reference-table entries with clinical significance.
- rs61751925Benignsingle nucleotide variant
- rs79487908Benignsingle nucleotide variant
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.