rs17879685

A SNP in the CYP2C19 gene on chromosome 10. Its most notable genotype is C;C: normal

Gene
CYP2C19
Location
Chr 1094,849,995 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, FamilyTreeDNA
Minor allele frequency
<1%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. C;CMost notableGoodnormalTypical · 0.097% of people
  2. C;TNot ratedcarrier of one CYP2C19*13 alleleTypical · 0.03% of people
  3. T;TNot ratedCYP2C19*13 homozygoteTypical · 0.00% of people

On SNPedia: (C;C), (C;T), (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Frequency

Share of each genotype in 8 HapMap populations.

  • AverageC;C 97% C;T 3% T;T 0%
  • Han Chinese (Beijing)C;C 99% C;T 2% T;T 0%
  • Yoruba (Nigeria)C;C 94% C;T 6% T;T 0%
  • African ancestry (Southwest US)C;C 97% C;T 4% T;T 0%
  • Gujarati IndianC;C 99% C;T 1% T;T 0%
  • Luhya (Kenya)C;C 92% C;T 8% T;T 0%
  • Mexican ancestry (Los Angeles)C;C 98% C;T 2% T;T 0%
  • Maasai (Kenya)C;C 97% C;T 3% T;T 0%
  • TuscanC;C 99% C;T 1% T;T 0%

Notes

From SNPedia

Notes

The rs17879685(T) SNP defines the CYP2C19 allele known as CYP2C19*13.

Source and license

Adapted from rs17879685 on SNPedia, using a snapshot taken October 16, 2026. SNPedia content is shared under CC BY-NC-SA 3.0 US, and this page is shared under the same license.

SNPedia is a community-edited wiki. Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice. Magnitude is a community rating of how interesting a genotype is, not a risk score.