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rs137852912(G;T)

From SNPedia
Dominant mutation associated with Familial Hypercholesterolemia
Is agenotype
ofrs137852912
GenePCSK9
Chromosome1
Position55,057,454
mentionedby
Magnitude4
ReputeBad
Geno Mag Summary
(G;G) 0 common in clinvar
(G;T) 4 Dominant mutation associated with Familial Hypercholesterolemia

Check cholesterol levels; if high, increased risk for cardiovascular disease