rs56144125(C;G)

Carrier of a CLN2 disease mutation

Magnitude
3.0Important
Repute
Bad
On SNPedia
rs56144125(C;G)
Gene
TPP1

Other genotypes of rs56144125

  1. C;CGoodcommon in clinvarTypical · 0.0
  2. G;GMost notableBadCLN2 disease (predicted)Very important · 8.8

All about rs56144125

Notes

From SNPedia

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

Source and license

Adapted from rs56144125(C;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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.