rs267606858(C;T)

Likely miscall in DNA chip data, such as that from Ancestry or 23andMe; otherwise, carrier of a glycogen storage disease mutation

Magnitude
3.0Important
Repute
Bad
On SNPedia
rs267606858(C;T)
Gene
GYG1

Other genotypes of rs267606858

  1. C;CGoodcommon in clinvarTypical · 0.0
  2. T;TMost notableBadLikely miscall in DNA-chip based data, such as that from Ancestry or 23andMe; otherwise, Glycogen storage disease XVVery important · 5.0

All about rs267606858

Notes

From SNPedia

Likely miscall in Ancestry and 23andMe data. When properly called, this genotype represents an unaffected carrier so long as there isn't another GYG1 mutation; see discussion at rs267606858

Source and license

Adapted from rs267606858(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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.