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rs869025453(-;CT)

From SNPedia

Dominant mutation associated with Familial Hypercholesterolemia
Is agenotype
ofrs869025453
GeneLDLR, MIR6886
Chromosome19
Position11,113,654
mentionedby
Magnitude4
ReputeBad
Geno Mag Summary
(-;CT) 4 Dominant mutation associated with Familial Hypercholesterolemia
(CT;CT) 0 common/normal