Gene entry
SLC22A1
solute carrier family 22 member 1
- Chromosome
- 6
- Cytoband
- 6q25.3
- Variants (rsID)
- 46
SLC22A1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 6 (region 6q25.3). Its official name is “solute carrier family 22 member 1”. The reference table lists 46 variants (rsID) for this gene.
Clinically classified variants
2 reference-table entries with clinical significance.
- rs628031Not classifiedmissense_variantLeukemia, Chronic Myeloid|Myeloid Leukemia|Type 2 Diabetes Mellitus|Diabetes Mellitus|Pure Autonomic Failure|Epilepsy|Polycystic Ovary Syndrome|Hypoglycemia|Telangiectasis|Ataxia and Polyneuropathy, Adult-Onset|Ataxia-Telangiectasia|Leukemia|Rem Sleep Behavior Disorder|Lipid Metabolism Disorder|Tremor
- rs683369Not classifiedmissense_variantLeukemia, Chronic Myeloid|Myeloid Leukemia|Primary Biliary Cholangitis|Biliary Cirrhosis, Primary, 1|Liver Cirrhosis|Leukemia|Polycystic Ovary Syndrome|Gastrointestinal Stromal Tumor|Esophageal Cancer|Toxic Shock Syndrome
Other listed variants
- rs461473
- rs594709
- rs609468
- rs622342
- rs644992
- rs662138
- rs806383
- rs1564348
- rs2197296
- rs2282142
- rs2282143
- rs2297373
- rs3822840
- rs4646278
- rs4646284
- rs6899549
- rs6935207
- rs7748057
- rs9347386
- rs9347389
- rs12208357
- rs34104736
- rs34108432
- rs34130495
- rs34205214
- rs34295611
- rs34447885
- rs34570655
- rs34888879
- rs35270274
- rs35373824
- rs35546288
- rs35888596
- rs35956182
- rs41267797
- rs57874120
- rs73025537
- rs77498589
- rs112476023
- rs117010682
- rs117307493
- rs118116045
- rs146534110
- rs201942835
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.