rs76151636(G;G)

Common in clinvar

Magnitude
0.0Typical
Repute
Good
On SNPedia
rs76151636(G;G)
Gene
ATP7B

Other genotypes of rs76151636

  1. G;TBadCarrier of a Wilson's disease mutationImportant · 3.0
  2. T;TMost notableBadWilson's disease; variable age of onsetVery important · 5.7

All about rs76151636

Source and license

Adapted from rs76151636(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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.