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rs375009082(G;G)

From SNPedia
common in clinvar
Is agenotype
ofrs375009082
GeneLDLR
Chromosome19
Position11,120,480
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;G) 2 Mutation of uncertain significance wrt to Familial Hypercholesterolemia
(G;G) 0 common in clinvar