rs119455955(A;G)

Carrier of a CLN2 mutation

Magnitude
3.0Important
Repute
Bad
On SNPedia
rs119455955(C;T)Minus strand
Gene
TPP1

Other genotypes of rs119455955

  1. G;GGoodcommon in clinvarTypical · 0.0
  2. A;AMost notableBadCLN2 disease (predicted)Very important · 8.8

All about rs119455955

Notes

From SNPedia

Unaffected in absence of a second mutation in the TPP1/CLN2 gene

Source and license

Adapted from rs119455955(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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.