rs2160519
A SNP in the GRIN2B gene on chromosome 12. Its most notable genotype is T;T: common on affy axiom data
- Gene
- GRIN2B
- Location
- Chr 1213,634,912 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 7%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs2160519 on the minus strand: (A;A). 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.
- AverageT;T 80%
- European ancestry (Utah)T;T 95%
- Han Chinese (Beijing)T;T 61%
- Japanese (Tokyo)T;T 65%
- Yoruba (Nigeria)T;T 100%
- Chinese (Denver)T;T 58%
- Gujarati IndianT;T 80%
- Maasai (Kenya)T;T 94%
- TuscanT;T 87%
Related
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 rs2160519 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.