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rs370777955(C;C)

From SNPedia

common in clinvar
Is agenotype
ofrs370777955
GeneLDLR, MIR6886
Chromosome19
Position11,113,643
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;C) 0 common in clinvar
(C;G) 4 Dominant mutation associated with Familial Hypercholesterolemia