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rs12713559(C;T)

From SNPedia

carrier of possible familial hypercholesterolemia mutation
Is agenotype
ofrs12713559
GeneAPOB
Chromosome2
Position21,006,196
Merged fromRs17241062
mentionedby
Magnitude3
ReputeBad
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 3 carrier of possible familial hypercholesterolemia mutation