Gene entry
SLC22A18
solute carrier family 67 member 1
- Chromosome
- 11
- Cytoband
- 11p15.4
- Variants (rsID)
- 43
SLC22A18 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 11 (region 11p15.4). Its official name is “solute carrier family 67 member 1”. The reference table lists 43 variants (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs367035Benignstart_lost
Other listed variants
- rs365605
- rs390266
- rs418439
- rs440150
- rs441258
- rs441286
- rs443193
- rs444198
- rs449318
- rs450208
- rs450876
- rs451443
- rs1048050
- rs1048054
- rs1048064
- rs1129782
- rs2237902
- rs4930027
- rs7950641
- rs10741735
- rs11024558
- rs11024580
- rs11024581
- rs12419420
- rs60292798
- rs72850026
- rs74840067
- rs76153913
- rs77275360
- rs113756608
- rs114817226
- rs139881375
- rs141445711
- rs141958733
- rs143044180
- rs146413382
- rs148116927
- rs149546938
- rs151047818
- rs184760249
- rs369789886
- rs533928834
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.