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rs121908043(A;C)

From SNPedia

Dominant mutation associated with Familial Hypercholesterolemia
Is agenotype
ofrs121908043
GeneLDLR, MIR6886
Chromosome19
Position11,113,307
mentionedby
Magnitude4
ReputeBad
Geno Mag Summary
(A;C) 4 Dominant mutation associated with Familial Hypercholesterolemia
(C;C) 0 common in clinvar
(C;T) 4 Dominant mutation associated with Familial Hypercholesterolemia