Abstract
Most genotyping arrays focus on common variants which only capture a fraction of genetic associations for a given trait. In contrast, the HumanExome Beadchip consists of mostly rare coding variants not on previous arrays. Eczema herpeticum (ADEH+) occurs from disseminated viral (HSV) infection and here, we genotyped the exome chip to identify functional coding variants associated with risk of ADEH+ as compared to uncomplicated AD (ADEH-).
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