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rs193922916(C;T)

From SNPedia
Carrier of an Alzheimer's disease mutation
Is agenotype
ofrs193922916
GeneAPP
Chromosome21
Position25,897,619
mentionedby
Magnitude3
ReputeBad
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 3 Carrier of an Alzheimer's disease mutation
(T;T) 7 significantly increased alzheimer's risk

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.