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rs137853965(C;C)

From SNPedia
dominant mutation leading to Familial Hypercholesterolemia
Is agenotype
ofrs137853965
GeneLDLR
Chromosome19
Position11,120,443
mentionedby
Magnitude4
Geno Mag Summary
(;) 0 common in clinvar
(-;-) 0 common in clinvar
(-;C) 5 Familial Hypercholesterolemia
(C;C) 4 dominant mutation leading to Familial Hypercholesterolemia