rs121908615

A SNP in the LITAF gene on chromosome 16. Its most notable genotype is C;T: Charcot-Marie-Tooth Disease, type 1

Gene
LITAF
Location
Chr 1611,549,693 (GRCh38)
Highest magnitude
6.1Very important
Tested on
AncestryDNA

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

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

SNPedia records rs121908615 on the minus strand: (A;G), (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Other LITAF SNPs

All LITAF SNPs

Source and license

Adapted from rs121908615 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.