Gene entry

SLC4A9

solute carrier family 4 member 9

Chromosome: 5
Cytoband: 5q31.3
Variants (rsID): 2

SLC4A9 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 5 (region 5q31.3). Its official name is “solute carrier family 4 member 9”. The reference table lists 2 variants (rsID) for this gene.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Clinically classified variants

1 reference-table entries with clinical significance.

rs6860077Not classifiedsplice_region_variant&synonymous_variantChiari Malformation Type I|Chiari Malformation

Other listed variants

rs55779592

Public references

NCBI Gene
Ensembl
ClinVar

Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.