rs760730366
A SNP in the MPZ gene on chromosome 1. Its most notable genotype is -;CCCGGGAG: Charcot-Marie-Tooth Disease, type 1
- Gene
- MPZ
- Location
- Chr 1161,307,356 (GRCh38)
- Highest magnitude
- 6.1Very important
- Tested on
- AncestryDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
- -;CCCGGGAGMost notableBadCharcot-Marie-Tooth Disease, type 1
- CCCGGGAG;CCCGGGAGGoodcommon in clinvar
On SNPedia: (-;CCCGGGAG), (CCCGGGAG;CCCGGGAG). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Other MPZ SNPs
- rs572010627A;TCharcot-Marie-Tooth (CMT) disease type 1B (predicted)Very important
- rs121913583C;TCharcot-Marie-Tooth Disease, type 1Very important
- rs121913584G;TCharcot-Marie-Tooth Disease, type 1Very important
- rs121913587A;GCharcot-Marie-Tooth Disease, type 1Very important
- rs121913588C;TCharcot-Marie-Tooth Disease, type 1Very important
- rs121913589C;GCharcot-Marie-Tooth Disease, type 1Very important
- rs121913590A;GCharcot-Marie-Tooth Disease, type 1Very important
- rs121913593A;GCharcot-Marie-Tooth Disease, type 1Very important
Source and license
Adapted from rs760730366 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.