rs58982919

A SNP in the NEFL gene on chromosome 8. Its most notable genotype is C;T: Charcot-Marie-Tooth Disease, type 1

Gene
NEFL
Location
Chr 824,956,223 (GRCh38)
Highest magnitude
6.1Very important
Tested on
23andMe, AncestryDNA

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. T;TGoodcommon in clinvarTypical · 0.0
  2. C;TMost notableBadCharcot-Marie-Tooth Disease, type 1Very important · 6.1

SNPedia records rs58982919 on the minus strand: (A;A), (A;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Other NEFL SNPs

All NEFL SNPs

Source and license

Adapted from rs58982919 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.