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rs121908038(T;T)

From SNPedia

common in complete genomics
Is agenotype
ofrs121908038
GeneLDLR, MIR6886
Chromosome19
Position11,113,293
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;T) 4 Dominant mutation associated with Familial Hypercholesterolemia
(T;T) 0 common in complete genomics