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rs137943601(A;G)

From SNPedia

Dominant mutation possibly associated with Familial Hypercholesterolemia
Is agenotype
ofrs137943601
GeneLDLR, MIR6886
Chromosome19
Position11,113,313
mentionedby
Magnitude4
ReputeBad
Geno Mag Summary
(A;G) 4 Dominant mutation possibly associated with Familial Hypercholesterolemia
(G;G) 0 common in clinvar

see discussion at rs137943601