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rs139617694(A;G)

From SNPedia
Dominant mutation associated with Familial Hypercholesterolemia
Is agenotype
ofrs139617694
GeneLDLR, MIR6886
Chromosome19
Position11,113,534
mentionedby
Magnitude5
ReputeBad
Geno Mag Summary
(A;G) 5 Dominant mutation associated with Familial Hypercholesterolemia
(G;G) 0 common in clinvar