rs2295814
A SNP in the EGR2 gene on chromosome 10. Its most notable genotype is G;G: common in complete genomics
- Gene
- EGR2
- Location
- Chr 1062,811,516 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- Not on consumer chips
- Minor allele frequency
- 8%
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 10 HapMap populations.
- AverageG;G 85%
- European ancestry (Utah)G;G 90%
- Han Chinese (Beijing)G;G 75%
- Japanese (Tokyo)G;G 73%
- Yoruba (Nigeria)G;G 100%
- African ancestry (Southwest US)G;G 98%
- Chinese (Denver)G;G 62%
- Gujarati IndianG;G 81%
- Mexican ancestry (Los Angeles)G;G 90%
- Maasai (Kenya)G;G 96%
- TuscanG;G 84%
Related
Other EGR2 SNPs
- rs104894159A;GCharcot-Marie-Tooth Disease, type 1Very important
- rs104894161A;GCharcot-Marie-Tooth Disease, type 1Very important
- rs281865137C;TCharcot-Marie-Tooth Disease, type 1Very important
- rs751448371C;TCharcot-Marie-Tooth Disease, type 1Very important
- rs879254278C;TCharcot-Marie-Tooth Disease, type 1Very important
- rs281865138C;CLikely miscall if from Ancestry data; otherwise, congenital hypomyelinating neuropathy mutationImportant
- rs10995315G;Gcommon in complete genomicsTypical
Source and license
Adapted from rs2295814 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.