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rs774069731(G;T)

From SNPedia

Dominant mutation associated with Familial Hypercholesterolemia
Is agenotype
ofrs774069731
GeneLDLR
Chromosome19
Position11,110,773
mentionedby
Magnitude4
ReputeBad
Geno Mag Summary
(G;T) 4 Dominant mutation associated with Familial Hypercholesterolemia
(T;T) 0 common/normal