41 research outputs found

    Estimated penetrance of identified SNPs for their corresponding phenotype

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    <p><b>Copyright information:</b></p><p>Taken from "Standard linkage and association methods identify the mechanism of four susceptibility genes for a simulated complex disease"</p><p></p><p>BMC Genetics 2005;6(Suppl 1):S142-S142.</p><p>Published online 30 Dec 2005</p><p>PMCID:PMC1866793.</p><p></p

    Incidence rates and race-specific hazard ratios (HR) for venous thromboembolism (VTE) in relation to quartiles of the 273-variant genetic risk score (GRS), ARIC*, 1987–2019.

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    Incidence rates and race-specific hazard ratios (HR) for venous thromboembolism (VTE) in relation to quartiles of the 273-variant genetic risk score (GRS), ARIC*, 1987–2019.</p

    Race-specific hazard ratios (HR) for venous thromboembolism (VTE) in relation to quartiles of the 273-variant genetic risk score (GRS) versus two supplemental GRSs, ARIC*, 1987–2019.

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    Race-specific hazard ratios (HR) for venous thromboembolism (VTE) in relation to quartiles of the 273-variant genetic risk score (GRS) versus two supplemental GRSs, ARIC*, 1987–2019.</p

    Fig 1 -

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    Hazard ratios of venous thromboembolism in relation to the 273-variant genetic risk score (GRS) in (a) White participants and (b) Black participants or the 5-Variant GRS in (c) White participants and (d) Black participants, ARIC, 1987–2019. Created using restricted cubic spline model with 3 knots and adjusted for age, sex, and principal components of ancestry. Reference values for the hazard ratios were 20.8 for the 273-variant score and 0.61 for the 5-variant score.</p
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