rs104894161
A SNP in the EGR2 gene on chromosome 10. Its most notable genotype is A;G: Charcot-Marie-Tooth Disease, type 1
- Gene
- EGR2
- Location
- Chr 1062,813,563 (GRCh38)
- Highest magnitude
- 6.1Very important
- Tested on
- AncestryDNA
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
- G;GGoodcommon in clinvar
- A;GMost notableBadCharcot-Marie-Tooth Disease, type 1
SNPedia records rs104894161 on the minus strand: (C;C), (C;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Other EGR2 SNPs
- rs104894159A;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
- rs2295814G;Gcommon in complete genomicsTypical
- rs10995315G;Gcommon in complete genomicsTypical
Source and license
Adapted from rs104894161 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.