rs28399504

A SNP in the CYP2C19 gene on chromosome 10. Its most notable genotype is G;G: poor metabolizer

Gene
CYP2C19
Location
Chr 1094,762,706 (GRCh38)
Highest magnitude
2.5Worth knowing
Tested on
23andMe, AncestryDNA, FamilyTreeDNA
Minor allele frequency
<1%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. A;AGoodnormalTypical · 0.098% of people
  2. A;GNot ratedcarrier of a CYP2C19*4 allele, considered a "slow metabolizer" variantWorth knowing · 2.02% of people
  3. G;GMost notableBadpoor metabolizerWorth knowing · 2.50% of people

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

Frequency

Share of each genotype in 2 HapMap populations.

  • AverageA;A 98% A;G 2% G;G 0%
  • Han Chinese (Beijing)A;A 99% A;G 2% G;G 0%
  • Mexican ancestry (Los Angeles)A;A 98% A;G 2% G;G 0%

Notes

From SNPedia

Show notes, about 130 words

rs28399504 is a SNP in the CYP2C19 gene, potentially encoding the CYP2C19*4 variant. This variant has been linked to poor metabolism of compounds like mephenytoin. It is also known as M1V or Met1Val. The risk allele is rs28399504(G). As a nonfunctioning CYP2C19, this variant would be expected to be a poor metabolizer of several commonly prescribed drugs, including anti-ulcer drugs like omeprazole (trade names Losec and Prilosec), esomeprazole (trade name Nexium), and lansoprazole (Prevacid). According to a 23andMe discussion This is one of the SNPs which were re-analyzed April 2009. Customers with older data may wish to redownload. SNPs effected rs4420638, rs34276300, rs3091244, rs34601266, rs2033003, rs7900194, rs9332239, rs28371685, rs1229984, and rs28399504. Clopidogrel Efficacy

Source and license

Adapted from rs28399504 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.