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rs121908042(C;G)

From SNPedia

Dominant mutation associated with Familial Hypercholesterolemia
Is agenotype
ofrs121908042
GeneLDLR
Chromosome19
Position11,105,232
mentionedby
Magnitude4
ReputeBad
Geno Mag Summary
(A;G) 4 Dominant mutation associated with Familial Hypercholesterolemia
(C;G) 4 Dominant mutation associated with Familial Hypercholesterolemia
(G;G) 0 common in clinvar