rs387906709(C;T)

Heterogenous neurodegeneration disorder

Magnitude
7.9Very important
Repute
Bad
On SNPedia
rs387906709(C;T)
Gene
UBQLN2

Other genotypes of rs387906709

  1. A;AMost notableBadAmyotrophic lateral sclerosis, type 15Very important · 7.9
  2. A;CBadAmyotrophic lateral sclerosis, type 15Very important · 7.9
  3. C;CGoodcommon in clinvarTypical · 0.0
  4. T;TBadHeterogeneous neurodegeneration disorderVery important · 7.9

All about rs387906709

Notes

From SNPedia

see rs387906709

Source and license

Adapted from rs387906709(C;T) 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.