rs16832015
A SNP on chromosome 1. Its most notable genotype is C;C: common in complete genomics
- Gene
- None listed
- Location
- Chr 1160,452,126 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe
- Minor allele frequency
- 3%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (C;C). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 8 HapMap populations.
- AverageC;C 93%
- European ancestry (Utah)C;C 99%
- Han Chinese (Beijing)C;C 88%
- Japanese (Tokyo)C;C 83%
- Yoruba (Nigeria)C;C 99%
- Chinese (Denver)C;C 90%
- Luhya (Kenya)C;C 99%
- Mexican ancestry (Los Angeles)C;C 90%
- TuscanC;C 99%
Notes
From SNPedia
Notes
non sig. gwas, hit (p = 2 x 10^-6) for intra-extra dimensional set shift (IED) EDS errors in the CANTAB (Cambridge Neuropsychological Test Automated Battery)
Source and license
Adapted from rs16832015 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.