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rs750649426(A;C)

From SNPedia

Dominant mutation associated with Familial Hypercholesterolemia
Is agenotype
ofrs750649426
GeneLDLR, MIR6886
Chromosome19
Position11,111,629
mentionedby
Magnitude4
ReputeBad
Geno Mag Summary
(A;C) 4 Dominant mutation associated with Familial Hypercholesterolemia
(C;C) 0 common/normal