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rs387906307(-;T)

From SNPedia

Dominant mutation associated with Familial Hypercholesterolemia
Is agenotype
ofrs387906307
GeneLDLR
Chromosome19
Position11,089,411
mentionedby
Magnitude4
ReputeBad
Geno Mag Summary
(-;T) 4 Dominant mutation associated with Familial Hypercholesterolemia
(T;T) 0 common in clinvar