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rs387906301(-;GCGATG)

From SNPedia

Dominant mutation associated with Familial Hypercholesterolemia
Is agenotype
ofrs387906301
GeneLDLR
Chromosome19
Position11,100,292
mentionedby
Magnitude4
ReputeBad
Geno Mag Summary
(-;GCGATG) 4 Dominant mutation associated with Familial Hypercholesterolemia
(GCGATG;GCGATG) 0 common in clinvar