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rs72658865(G;T)

From SNPedia

Dominant mutation associated with Familial Hypercholesterolemia
Is agenotype
ofrs72658865
GeneLDLR
Chromosome19
Position11,116,969
mentionedby
Magnitude4
ReputeBad
Geno Mag Summary
(G;G) 0 common in clinvar
(G;T) 4 Dominant mutation associated with Familial Hypercholesterolemia