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rs193922567(A;T)

From SNPedia

Dominant mutation associated with Familial Hypercholesterolemia
Is agenotype
ofrs193922567
GeneLDLR, MIR6886
Chromosome19
Position11,113,451
mentionedby
Magnitude4
ReputeBad
Geno Mag Summary
(A;T) 4 Dominant mutation associated with Familial Hypercholesterolemia
(T;T) 0 common in clinvar