rs11066015
A SNP in the ACAD10 gene on chromosome 12. Its most notable genotype is G;G: common in complete genomics
- Gene
- ACAD10
- Location
- Chr 12111,730,205 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 6%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 6 HapMap populations.
- AverageG;G 80%
- European ancestry (Utah)G;G 100%
- Han Chinese (Beijing)G;G 71%
- Japanese (Tokyo)G;G 60%
- Chinese (Denver)G;G 54%
- Gujarati IndianG;G 99%
- Mexican ancestry (Los Angeles)G;G 97%
Related
Genosets
- Gs2454x increased risk for esophageal squamous cell cancer among Han ChineseVery important
- Gs2442x increased risk for esophageal squamous cell cancer among Han ChineseWorth knowing
Genosets combine several genotypes. Twofold checks them in your report.
Source and license
Adapted from rs11066015 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.