rs121909667(G;G)

Causing ALS AMYOTROPHIC LATERAL SCLEROSIS

Magnitude
6.0Very important
Repute
Bad
On SNPedia
rs121909667(G;G)
Gene
FUS

Other genotypes of rs121909667

  1. C;CGoodcommon in clinvarTypical · 0.0

All about rs121909667

Notes

From SNPedia

AMYOTROPHIC LATERAL SCLEROSIS 6 In 4 affected members of a consanguineous family with amyotrophic lateral sclerosis-6 (ALS6; 608030), Kwiatkowski et al. (2009) identified a homozygous 1551C-G transversion in exon 15 of the FUS gene, resulting in a his517-to-gln (H517Q) substitution. The family originated from Cape Verde, a small island off the western coast of Africa. Three asymptomatic family members were also homozygous for the mutation, but all were younger than the mean age at disease onset of 45 years. The mutation was not detected in 1,446 control DNA samples from North America; 1 heterozygote was observed in 132 chromosomes from Cape Verde.

Source and license

Adapted from rs121909667(G;G) 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.