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rs137853964(A;G)

From SNPedia
Variant of uncertain status wrt Familial Hypercholesterolemia
Is agenotype
ofrs137853964
GeneLDLR
Chromosome19
Position11,129,602
mentionedby
Magnitude2
Geno Mag Summary
(A;G) 2 Variant of uncertain status wrt Familial Hypercholesterolemia
(G;G) 0 common in clinvar
(G;T) 5 Familial Hypercholesterolemia

See discussion at rs137853964 regarding 'second' variant, c.2479G>A