rs12713559(C;C)

common in clinvar

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

Magnitude

0

Repute

Good

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