rs12012519
A SNP on chromosome X. Its most notable genotype is T;T: common on affy axiom data
- Gene
- None listed
- Location
- Chr X87,935,349 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 7%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 7 HapMap populations.
- AverageT;T 87%
- European ancestry (Utah)T;T 100%
- Han Chinese (Beijing)T;T 73%
- Japanese (Tokyo)T;T 92%
- Yoruba (Nigeria)T;T 76%
- Chinese (Denver)T;T 82%
- Gujarati IndianT;T 92%
- Mexican ancestry (Los Angeles)T;T 98%
Notes
From SNPedia
Notes
Genome-wide association study SNPs in the human genome diversity project populations: does selection affect unlinked SNPs with shared trait associations?
Source and license
Adapted from rs12012519 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.