Barely Significant
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The genetic variation rs12143842 in NOS1AP increases idiopathic ventricular tachycardia risk in Chinese Han populations.

Sci Rep · 2017 · PMC5567283 · PMID 28827735

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highly significantno p-value reported
Both allelic and genotypic association between SNP rs12143842 and IVT remained highly significant after adjusting for age and gender (Tables 2 and 3 ).

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