rs199422214
A SNP in the NEFL gene on chromosome 8. Its most notable genotype is A;C: Charcot-Marie-Tooth Disease, type 1
- Gene
- NEFL
- Location
- Chr 824,955,888 (GRCh38)
- Highest magnitude
- 6.1Very important
- Tested on
- AncestryDNA
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
- C;CGoodcommon in clinvar
- A;CMost notableBadCharcot-Marie-Tooth Disease, type 1
SNPedia records rs199422214 on the minus strand: (G;G), (G;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Source and license
Adapted from rs199422214 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.