rs4344
A SNP in the ACE gene on chromosome 17. Its most notable genotype is A;A: faster responder
- Gene
- ACE
- Location
- Chr 1763,489,363 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, FamilyTreeDNA
- Minor allele frequency
- 49%
Genotypes
As shown in 23andMe and AncestryDNA files.
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 11 HapMap populations.
- AverageA;A 26% A;G 48% G;G 25%
- European ancestry (Utah)A;A 27% A;G 47% G;G 27%
- Han Chinese (Beijing)A;A 53% A;G 39% G;G 8%
- Japanese (Tokyo)A;A 33% A;G 51% G;G 16%
- Yoruba (Nigeria)A;A 15% A;G 50% G;G 35%
- African ancestry (Southwest US)A;A 5% A;G 67% G;G 28%
- Chinese (Denver)A;A 41% A;G 49% G;G 10%
- Gujarati IndianA;A 35% A;G 51% G;G 15%
- Luhya (Kenya)A;A 19% A;G 48% G;G 33%
- Mexican ancestry (Los Angeles)A;A 41% A;G 35% G;G 24%
- Maasai (Kenya)A;A 9% A;G 51% G;G 40%
- TuscanA;A 12% A;G 44% G;G 44%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
This SNP in the ACE gene, also known as G12269A, is reported to influence how quickly African Americans respond to the anti-hypertensive drug ramipril. rs4344(A;A) and rs4344(G;G) homozygotes are able to reach lower blood pressure levels upon treatment with ramipril sooner than rs4344(A;G) heterozygotes. The odds ratio reported for this study, comparing both homozygotes to heterozygotes, is 1.86 (CI: 1.32-3.23). Note that this SNP is in almost complete linkage disequilibrium with the insertion/deletion ACE gene SNP.
G;G
Faster responder to ACE inhibitor Ramipril Altace.
Source and license
Adapted from rs4344 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.