Best TWAS P=5.438581e-10 · Best GWAS P=8.877452e-12 conditioned to 2.703087e-05
# | Tissue | Gene | Modality | RNA phenotype | h2 | eQTL R2 | model | # weights | model R2 | model R2 P | eQTL GWAS Z | TWAS Z | TWAS P | Top SNP corr | PP3 | PP4 | joint |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
1 | BLA | Med30 | gene expression | ENSRNOG00000004844 | 0.07 | 0.04 | blup | 1914 | 0.05 | 1.3e-03 | -4.9 | -5.3 | 1.1e-07 | 0.59 | 0.46 | 0.42 | FALSE |
2 | BLA | Ext1 | mRNA stability | ENSRNOG00000024886 | 0.38 | 0.26 | blup | 1844 | 0.29 | 1.2e-15 | -4.3 | 5.2 | 1.7e-07 | -0.56 | 0.37 | 0.63 | FALSE |
3 | Brain | Trps1 | gene expression | ENSRNOG00000024998 | 0.06 | 0.05 | blup | 1999 | 0.07 | 8.2e-07 | -3.4 | 5.5 | 4.2e-08 | -0.86 | 0.52 | 0.48 | FALSE |
4 | Brain | Med30 | mRNA stability | ENSRNOG00000004844 | 0.04 | 0.00 | blup | 1914 | 0.02 | 4.3e-03 | -5.0 | 6.2 | 5.4e-10 | -0.52 | 0.46 | 0.43 | TRUE |
5 | Brain | Ext1 | mRNA stability | ENSRNOG00000024886 | 0.10 | 0.08 | blup | 1844 | 0.09 | 6.9e-09 | 4.1 | 5.4 | 5.8e-08 | -0.56 | 0.44 | 0.56 | FALSE |
6 | LHb | Rad21 | gene expression | ENSRNOG00000004420 | 0.22 | 0.11 | lasso | 2 | 0.12 | 1.1e-03 | -4.9 | -5.9 | 4.1e-09 | 0.61 | 0.48 | 0.38 | FALSE |
7 | Liver | Med30 | intron excision ratio | chr7:84012067:84015230 | 0.06 | 0.02 | enet | 68 | 0.02 | 1.1e-03 | -4.7 | -5.8 | 7.4e-09 | 0.37 | 0.60 | 0.23 | FALSE |
8 | PL | Ext1 | mRNA stability | ENSRNOG00000024886 | 0.27 | 0.02 | blup | 1838 | 0.11 | 1.5e-03 | 4.2 | 5.3 | 1.1e-07 | -0.51 | 0.44 | 0.33 | FALSE |
9 | PL2 | Trps1 | gene expression | ENSRNOG00000024998 | 0.05 | 0.05 | top1 | 1 | 0.05 | 1.7e-03 | -5.1 | 5.1 | 2.9e-07 | -0.87 | 0.09 | 0.04 | FALSE |
10 | PL2 | Ext1 | mRNA stability | ENSRNOG00000024886 | 0.62 | 0.41 | enet | 236 | 0.45 | 1.3e-26 | -4.7 | 5.4 | 8.3e-08 | -0.58 | 0.31 | 0.69 | FALSE |
h2: Heritability estimate for the given transcriptomic model. PP3: Posterior probability of two distinct causal variants. PP4: Posterior probability of a single shared causal variant. joint: Whether the RNA phenotype is in the joint model.