rs137853280(C;G)

Unaffected carrier of a Wilson disease mutation

Magnitude
3.0Important
Repute
Bad
On SNPedia
rs137853280(C;G)Minus strand
Gene
ATP7B

Other genotypes of rs137853280

  1. G;GGoodcommon in clinvarTypical · 0.0
  2. C;CGoodcommon in clinvarTypical · 0.0
  3. A;CBadUnaffected carrier of a Wilson disease mutationImportant · 3.0

All about rs137853280

Notes

From SNPedia

Unaffected in absence of a second ATP7B gene mutation; see links via main rs-page.

Source and license

Adapted from rs137853280(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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.