Gene entry
SLC22A4
solute carrier family 22 member 4
- Chromosome
- 5
- Cytoband
- 5q31.1
- Variants (rsID)
- 34
SLC22A4 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 5 (region 5q31.1). Its official name is “solute carrier family 22 member 4”. The reference table lists 34 variants (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs1050152Benignsingle nucleotide variantSLC22A4 POLYMORPHISM
Other listed variants
- rs272869
- rs272873
- rs272885
- rs272889
- rs273909
- rs273913
- rs273914
- rs398064
- rs419291
- rs582849
- rs679793
- rs679896
- rs680124
- rs3761660
- rs3828671
- rs4646201
- rs6860806
- rs11568500
- rs11568501
- rs11568509
- rs11568510
- rs11950562
- rs13179900
- rs17852518
- rs28626351
- rs56399423
- rs116591686
- rs143140136
- rs147195274
- rs150135214
- rs184981826
- rs201371114
- rs201521490
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.