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Gene entry

CYP2C8

cytochrome P450 family 2 subfamily C member 8

Chromosome
10
Cytoband
10q23.33
Variants (rsID)
32

CYP2C8 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 10 (region 10q23.33). Its official name is “cytochrome P450 family 2 subfamily C member 8”. The reference table lists 32 variants (rsID) for this gene.

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Clinically classified variants

4 reference-table entries with clinical significance.

  • rs1058930Benignsingle nucleotide variantCYP2C8 POLYMORPHISM
  • rs11572103Benignsingle nucleotide variantCYP2C8 POLYMORPHISM
  • rs2071426Benignsingle nucleotide variant
  • rs11572080Othersingle nucleotide variantMacular Degeneration, Age-Related, 1|Glucocorticoid Deficiency 4 with or Without Mineralocorticoid Deficiency|Peripheral Nervous System Disease|Neuropathy|Myeloid Leukemia|Helicobacter Pylori Infection|Leukemia|Myocardial Infarction|Gastrointestinal Stromal Tumor|Leukemia, Chronic Myeloid|Thrombocytopenic Purpura, Autoimmune|Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets|Peptic Ulcer Disease|Purpura

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.