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rs387906306(-;TGCAAGGACAAATCTGAC)

From SNPedia

Dominant mutation associated with Familial Hypercholesterolemia
Is agenotype
ofrs387906306
GeneLDLR
Chromosome19
Position11,105,587
mentionedby
Magnitude4
ReputeBad
Geno Mag Summary
(;) 0 common in clinvar
(-;TGCAAGGACAAATCTGAC) 4 Dominant mutation associated with Familial Hypercholesterolemia