rs104894617
A SNP in the PMP22 gene on chromosome 17. Its most notable genotype is A;G: Charcot-Marie-Tooth Disease, type 1
- Gene
- PMP22
- Location
- Chr 1715,260,681 (GRCh38)
- Highest magnitude
- 6.1Very important
- Tested on
- AncestryDNA
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
- A;GMost notableBadCharcot-Marie-Tooth Disease, type 1
- A;AGoodcommon in clinvar
SNPedia records rs104894617 on the minus strand: (C;T), (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Other PMP22 SNPs
- rs104894618C;GCharcot-Marie-Tooth Disease, type 1Very important
- rs104894621A;GCharcot-Marie-Tooth Disease, type 1Very important
- rs104894625A;GCharcot-Marie-Tooth Disease, type 1Very important
- rs104894627A;TCharcot-Marie-Tooth Disease, type 1Very important
- rs863225027A;TCharcot-Marie-Tooth Disease, type 1Very important
- rs863225028G;TCharcot-Marie-Tooth Disease, type 1Very important
- rs863225029-;ACharcot-Marie-Tooth Disease, type 1Very important
- rs13422T;Tcommon in clinvarTypical
Source and license
Adapted from rs104894617 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.