rs11225297
A SNP on chromosome 11. Its most notable genotype is A;A.
- Gene
- None listed
- Location
- Chr 11102,517,147 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe
- Minor allele frequency
- 11%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (A;A). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 10 HapMap populations.
- AverageA;A 79%
- European ancestry (Utah)A;A 77%
- Han Chinese (Beijing)A;A 65%
- Japanese (Tokyo)A;A 70%
- Yoruba (Nigeria)A;A 99%
- African ancestry (Southwest US)A;A 98%
- Chinese (Denver)A;A 60%
- Gujarati IndianA;A 87%
- Mexican ancestry (Los Angeles)A;A 66%
- Maasai (Kenya)A;A 96%
- TuscanA;A 78%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
Chinese breast cancer rs11225297(T) improved survival. (A;T) (OS HR: 0.7, 95% CI: 0.5-0.9) and (T;T) (OS HR: 0.3, 95% CI: 0.1-0.8)
Source and license
Adapted from rs11225297 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.