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rs778309692(C;G)

From SNPedia

Dominant mutation associated with Familial Hypercholesterolemia
Is agenotype
ofrs778309692
GeneLDLR, MIR6886
Chromosome19
Position11,113,390
mentionedby
Magnitude4
ReputeBad
Geno Mag Summary
(C;C) 0 common/normal
(C;G) 4 Dominant mutation associated with Familial Hypercholesterolemia