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rs767618089(A;G)

From SNPedia

Dominant mutation associated with Familial Hypercholesterolemia
Is agenotype
ofrs767618089
GeneLDLR
Chromosome19
Position11,107,472
mentionedby
Magnitude4
ReputeBad
Geno Mag Summary
(A;A) 0 common/normal
(A;G) 4 Dominant mutation associated with Familial Hypercholesterolemia