rs28930068(T;T)

Hypokalemic periodic paralysis risk

Magnitude
5.0Very important
Repute
Bad
On SNPedia
rs28930068(A;A)Minus strand
Gene
CACNA1S

Other genotypes of rs28930068

  1. C;TMost notableBadMalignant Hyperthermia susceptibilityVery important · 6.6
  2. C;CGoodcommon in clinvarTypical · 0.0

All about rs28930068

Notes

From SNPedia

Hypokalemic periodic paralysis (hypoKPP) is an autosomal dominant skeletal muscle disorder, so carriers of even one rs28930068(G) allele are at risk for this disorder.

Source and license

Adapted from rs28930068(A;A) 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.