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rs778408161(C;T)

From SNPedia

Dominant mutation associated with Familial Hypercholesterolemia
Is agenotype
ofrs778408161
GeneLDLR
Chromosome19
Position11,117,000
mentionedby
Magnitude4
ReputeBad
Geno Mag Summary
(C;T) 4 Dominant mutation associated with Familial Hypercholesterolemia
(T;T) 0 common/normal