rs1801272

A SNP in the CYP2A6 gene on chromosome 19. Its most notable genotype is T;T: Reduced CYP2A6 metabolism; impaired nicotine metabolism?

Gene
CYP2A6
Location
Chr 1940,848,628 (GRCh38)
Highest magnitude
2.0Worth knowing
Tested on
23andMe, AncestryDNA
Minor allele frequency
1%

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. T;TMost notableNot ratedReduced CYP2A6 metabolism; impaired nicotine metabolism?Worth knowing · 2.00% of people
  2. A;TNot ratedReduced CYP2A6 metabolism; impaired nicotine metabolism?Minor · 1.03% of people
  3. A;AGoodcommon in clinvarTypical · 0.097% of people

SNPedia records rs1801272 on the minus strand: (A;A), (A;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 4 HapMap populations.

  • AverageT;T 0% A;T 3% A;A 97%
  • European ancestry (Utah)T;T 0% A;T 9% A;A 91%
  • Han Chinese (Beijing)T;T 0% A;T 0% A;A 100%
  • Japanese (Tokyo)T;T 0% A;T 5% A;A 96%
  • Yoruba (Nigeria)T;T 0% A;T 0% A;A 100%

Notes

From SNPedia

Notes

minor form is a slow metaboliser according to pharmgkb

Source and license

Adapted from rs1801272 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.