Gene entry
SLC9A6
solute carrier family 9 member A6
- Chromosome
- X
- Cytoband
- Xq26.3
- Variants (rsID)
- 24
SLC9A6 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome X (region Xq26.3). Its official name is “solute carrier family 9 member A6”. The reference table lists 24 variants (rsID) for this gene.
Clinically classified variants
10 reference-table entries with clinical significance.
- rs146263125Benignsingle nucleotide variantHistory of neurodevelopmental disorder|Christianson syndrome|Intellectual disability
- rs2307131Benignsingle nucleotide variantChristianson syndrome|History of neurodevelopmental disorder
- rs563279759Benignsingle nucleotide variantChristianson syndrome
- rs190788663Conflicting interpretationssingle nucleotide variant
- rs886044780Conflicting interpretationssingle nucleotide variantChristianson syndrome
- rs139299794Likely benignsingle nucleotide variantChristianson syndrome
- rs122461162Pathogenicsingle nucleotide variantChristianson syndrome
- rs398122849PathogenicDeletionChristianson syndrome
- rs398123003Pathogenicsingle nucleotide variantChristianson syndrome
- rs796053290PathogenicDeletionIntellectual disability|Christianson 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.