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Lack of association between classical HLA genes and asymptomatic SARS-CoV-2 infection
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Discovery of new myositis genetic associations through leveraging other immune-mediated diseases
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Toward reporting standards for the pathogenicity of variant combinations involved in multilocus/oligogenic diseases
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Biallelic variants in MESD, which encodes a WNT-signaling-related protein, in four new families with recessively inherited osteogenesis imperfecta