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rs139617694(G;G)

From SNPedia

common in clinvar
Is agenotype
ofrs139617694
GeneLDLR, MIR6886
Chromosome19
Position11,113,534
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;G) 4 Dominant mutation associated with Familial Hypercholesterolemia
(G;G) 0 common in clinvar