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rs200238879(T;T)

From SNPedia

common in clinvar
Is agenotype
ofrs200238879
GeneLDLR
Chromosome19
Position11,105,602
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;T) 4 Dominant mutation associated with Familial Hypercholesterolemia
(T;T) 0 common in clinvar