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Gene entry

CYP2C19

cytochrome P450 family 2 subfamily C member 19

Chromosome
10
Cytoband
10q23.33
Variants (rsID)
66

CYP2C19 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 19”. The reference table lists 66 variants (rsID) for this gene.

Clinically classified variants

20 reference-table entries with clinical significance.

  • rs118203756Drug responsesingle nucleotide variantCYP2C19: uncertain function
  • rs118203759Drug responsesingle nucleotide variantCYP2C19: decreased function
  • rs12248560Drug responsesingle nucleotide variantCYP2C19: increased function
  • rs12769205Drug responsesingle nucleotide variantCYP2C19: no function
  • rs1288601658Drug responsesingle nucleotide variantCYP2C19: uncertain function
  • rs138142612Drug responsesingle nucleotide variantCYP2C19: normal function
  • rs140278421Drug responsesingle nucleotide variantCYP2C19: no function
  • rs145328984Drug responsesingle nucleotide variantCYP2C19: uncertain function
  • rs17879685Drug responsesingle nucleotide variantCYP2C19: normal function
  • rs375781227Drug responsesingle nucleotide variantCYP2C19: decreased function
  • rs41291556Drug responsesingle nucleotide variantCYP2C19: no function
  • rs4986893Drug responsesingle nucleotide variantMephenytoin, poor metabolism of|Proguanil, poor metabolism of|CYP2C19: no function|Acute coronary syndrome
  • rs55640102Drug responsesingle nucleotide variantCYP2C19: uncertain function
  • rs56337013Drug responsesingle nucleotide variantMephenytoin, poor metabolism of|CYP2C19: no function
  • rs72552267Drug responsesingle nucleotide variantCYP2C19: no function
  • rs72558186Drug responsesingle nucleotide variantCYP2C19: no function
  • rs7902257Drug responsesingle nucleotide variantCYP2C19: uncertain function
  • rs111490789Othersingle nucleotide variant
  • rs113164681Othersingle nucleotide variant
  • rs118203757Othersingle nucleotide variant

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.