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Gene entry

SLC22A2

solute carrier family 22 member 2

Chromosome
6
Cytoband
6q25.3
Variants (rsID)
29

SLC22A2 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 2”. The reference table lists 29 variants (rsID) for this gene.

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Clinically classified variants

3 reference-table entries with clinical significance.

  • rs316003Not classifiedsynonymous_variant
  • rs316019Not classifiedmissense_variantLactic Acidosis|Anoxia|Sensorineural Hearing Loss|Wolfram Syndrome 1|Lung Cancer|Type 2 Diabetes Mellitus|Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus|Diabetes Mellitus|Testicular Cancer|Branchiootic Syndrome 1|Polycystic Ovary Syndrome|Body Mass Index Quantitative Trait Locus 1|Type 1 Diabetes Mellitus|Colorectal Cancer|Rheumatoid Arthritis|Microvascular Complications of Diabetes 6|Microvascular Complications of Diabetes 4|Microvascular Complications of Diabetes 3
  • rs624249Not classifiedsynonymous_variantRheumatoid Arthritis|Arthritis

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.