rs193922916(A;G)

Carrier of an Alzheimer's disease mutation

Magnitude
3.0Important
Repute
Bad
On SNPedia
rs193922916(C;T)Minus strand
Gene
APP

Other genotypes of rs193922916

  1. G;GGoodcommon in clinvarTypical · 0.0
  2. A;AMost notableBadsignificantly increased alzheimer's riskVery important · 7.0

All about rs193922916

Notes

From SNPedia

Likely to be unaffected in absence of another APP or Alzheimer mutation, as this mutation appears to be inherited recessively. See rs193922916 for more information.

Source and license

Adapted from rs193922916(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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.