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rs3918242(C;T)
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1.14x increased risk for MI; also check haplotype
Is a
genotype
of
rs3918242
Gene
MMP9
Chromosome
20
Position
46,007,337
mentioned
by
Geno
Mag
Summary
(C;C)
normal risk
(C;T)
1.14x increased risk for MI; also check haplotype
(T;T)
1.33x increased risk for MI; also check haplotype
Category
:
Is a genotype
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