p value Search Results


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MYH9 association analysis results in the Wake Forest sample (25 SLE-ESRD cases vs. 735 non-SLE controls)
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MYH9 association analysis results in the Wake Forest sample (25 SLE-ESRD cases vs. 735 non-SLE controls)
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MYH9 association analysis results in the Wake Forest sample (25 SLE-ESRD cases vs. 735 non-SLE controls)
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MYH9 association analysis results in the Wake Forest sample (25 SLE-ESRD cases vs. 735 non-SLE controls)
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MYH9 association analysis results in the Wake Forest sample (25 SLE-ESRD cases vs. 735 non-SLE controls)
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MYH9 association analysis results in the Wake Forest sample (25 SLE-ESRD cases vs. 735 non-SLE controls)
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MYH9 association analysis results in the Wake Forest sample (25 SLE-ESRD cases vs. 735 non-SLE controls)
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MYH9 association analysis results in the Wake Forest sample (25 SLE-ESRD cases vs. 735 non-SLE controls)
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MYH9 association analysis results in the Wake Forest sample (25 SLE-ESRD cases vs. 735 non-SLE controls)
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ChemAxon LLC log p value generator
MYH9 association analysis results in the Wake Forest sample (25 SLE-ESRD cases vs. 735 non-SLE controls)
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CH Instruments cb2 chi-squared p value
MYH9 association analysis results in the Wake Forest sample (25 SLE-ESRD cases vs. 735 non-SLE controls)
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Image Search Results


MYH9 association analysis results in the Wake Forest sample (25 SLE-ESRD cases vs. 735 non-SLE controls)

Journal: American Journal of Nephrology

Article Title: The Non-Muscle Myosin Heavy Chain 9 Gene (MYH9) Is Not Associated with Lupus Nephritis in African Americans

doi: 10.1159/000314688

Figure Lengend Snippet: MYH9 association analysis results in the Wake Forest sample (25 SLE-ESRD cases vs. 735 non-SLE controls)

Article Snippet: SNP genotyping was performed on a TaqMan Genotyping System (Applied Biosystems, Carlsbad, Calif., USA). table ft1 table-wrap mode="anchored" t5 Table 2 caption a7 Marker Risk allele Minor allele frequency HWE p value Recessive test cases controls cases controls OR 95% CI p value rs11912763 A 0.28 0.19 0.30 0.47 4.31 1.14, 16.34 0.0319 rs4821480 G 0.76 0.61 0.07 0.10 2.60 1.06, 6.37 0.0361 rs2032487 C 0.75 0.62 0.11 0.11 2.37 1.00, 5.62 0.0496 rs4821481 C 0.77 0.61 0.06 0.12 2.82 1.16, 6.84 0.0217 rs5750250 A 0.35 0.49 1.00 0.88 0.56 0.16, 1.93 0.3577 rs3752462 T 0.85 0.73 0.43 0.25 2.06 0.79, 5.35 0.1398 rs5756152 A 0.35 0.25 1.00 1.00 1.78 0.50, 6.40 0.3757 Open in a separate window MYH9 association analysis results in the Wake Forest sample (25 SLE-ESRD cases vs. 735 non-SLE controls) Seventy di-allelic ancestry informative markers (AIMs) were genotyped to provide individual admixture proportion estimates used to control for population substructure in the association tests from the WFUSM samples (AIM genotypes were not available in the NIH samples).

Techniques:

MYH9 association analysis in PROFILE participants with principal component data (300 LN cases vs. 246 SLE non-nephropathy controls)

Journal: American Journal of Nephrology

Article Title: The Non-Muscle Myosin Heavy Chain 9 Gene (MYH9) Is Not Associated with Lupus Nephritis in African Americans

doi: 10.1159/000314688

Figure Lengend Snippet: MYH9 association analysis in PROFILE participants with principal component data (300 LN cases vs. 246 SLE non-nephropathy controls)

Article Snippet: SNP genotyping was performed on a TaqMan Genotyping System (Applied Biosystems, Carlsbad, Calif., USA). table ft1 table-wrap mode="anchored" t5 Table 2 caption a7 Marker Risk allele Minor allele frequency HWE p value Recessive test cases controls cases controls OR 95% CI p value rs11912763 A 0.28 0.19 0.30 0.47 4.31 1.14, 16.34 0.0319 rs4821480 G 0.76 0.61 0.07 0.10 2.60 1.06, 6.37 0.0361 rs2032487 C 0.75 0.62 0.11 0.11 2.37 1.00, 5.62 0.0496 rs4821481 C 0.77 0.61 0.06 0.12 2.82 1.16, 6.84 0.0217 rs5750250 A 0.35 0.49 1.00 0.88 0.56 0.16, 1.93 0.3577 rs3752462 T 0.85 0.73 0.43 0.25 2.06 0.79, 5.35 0.1398 rs5756152 A 0.35 0.25 1.00 1.00 1.78 0.50, 6.40 0.3757 Open in a separate window MYH9 association analysis results in the Wake Forest sample (25 SLE-ESRD cases vs. 735 non-SLE controls) Seventy di-allelic ancestry informative markers (AIMs) were genotyped to provide individual admixture proportion estimates used to control for population substructure in the association tests from the WFUSM samples (AIM genotypes were not available in the NIH samples).

Techniques: