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Figure 1.
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- Gan et al., 2026 - COMMD9-regulated endothelial cell abnormality-induced hypercoagulability is associated with Budd-Chiari syndrome
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Figure 1.
Exome-wide association analysis. Gene-level P-values were generated using SKAT analysis in the BCS group. (A) No genes demonstrated a significant association with the disease based on SKAT analysis. The blue line indicates the threshold of P = 1.43e−06. (B) Quantile-quantile plots based on P-values from SKAT analysis assessing the burden of rare variants (MAF < 0.01). (C) Variant frequencies of KLHDC2 are higher than those of JAK2 and MTHFR between the BCS and control samples. (D) The overlap of significant genes via the SKAT analysis on the burden of rare variants between the BCS and VaMs cohorts.
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