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rs12713559(C;T)

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carrier of possible familial hypercholesterolemia mutation

Is a	genotype
of	rs12713559
Gene	APOB
Chromosome	2
Position	21,006,196
Merged from	Rs17241062
mentioned	by

3

Bad

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;T)	3	carrier of possible familial hypercholesterolemia mutation

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Is a genotype