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rs121908031(A;C)

From SNPedia

Dominant mutation associated with Familial Hypercholesterolemia
Is agenotype
ofrs121908031
GeneLDLR
Chromosome19
Position11,120,425
mentionedby
Magnitude4
ReputeBad
Geno Mag Summary
(A;C) 4 Dominant mutation associated with Familial Hypercholesterolemia
(C;C) 0 common in complete genomics