Best TWAS P=4.644272e-10 · Best GWAS P=1.219209e-06 conditioned to 0.003040115
# | 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 | Adipose | Jade1 | gene expression | ENSRNOG00000014066 | 0.13 | 0.01 | blup | 1263 | 0.04 | 4.2e-05 | -3.9 | 5.8 | 5.9e-09 | -0.78 | 0.52 | 0.44 | FALSE |
2 | Brain | Jade1 | alternative polyA | ENSRNOT00000018872 | 0.20 | 0.06 | enet | 116 | 0.09 | 1.3e-08 | 3.8 | 6.2 | 4.6e-10 | -0.33 | 0.77 | 0.21 | TRUE |
3 | Brain | Jade1 | alternative polyA | ENSRNOT00000100298 | 0.20 | 0.06 | enet | 115 | 0.09 | 1.5e-08 | 3.8 | -6.2 | 6.9e-10 | 0.25 | 0.76 | 0.21 | FALSE |
4 | Brain | Larp1b | alternative TSS | ENSRNOT00000044804 | 0.06 | 0.03 | enet | 31 | 0.03 | 3.7e-04 | 4.1 | 6.1 | 8.8e-10 | -0.51 | 0.34 | 0.54 | FALSE |
5 | Brain | Jade1 | isoform ratio | ENSRNOT00000018872 | 0.08 | 0.00 | enet | 39 | 0.01 | 3.0e-02 | 4.1 | 6.2 | 4.9e-10 | -0.40 | 0.14 | 0.12 | FALSE |
6 | Brain | Jade1 | isoform ratio | ENSRNOT00000100298 | 0.22 | 0.07 | enet | 107 | 0.09 | 9.3e-09 | 3.8 | -5.7 | 1.1e-08 | 0.05 | 0.78 | 0.20 | FALSE |
7 | Brain | Larp1b | isoform ratio | ENSRNOT00000044804 | 0.09 | 0.05 | enet | 36 | 0.05 | 1.2e-05 | 4.1 | 6.2 | 6.5e-10 | -0.59 | 0.36 | 0.60 | FALSE |
8 | Brain | RGD1359508 | mRNA stability | ENSRNOG00000038330 | 0.11 | 0.11 | enet | 99 | 0.12 | 3.5e-11 | -4.4 | -5.1 | 2.8e-07 | 0.90 | 0.43 | 0.56 | FALSE |
9 | Liver | RGD1565989 | gene expression | ENSRNOG00000013940 | 0.09 | 0.02 | enet | 37 | 0.02 | 1.1e-03 | 3.5 | -5.4 | 6.3e-08 | 0.07 | 0.51 | 0.35 | FALSE |
10 | PL2 | Jade1 | gene expression | ENSRNOG00000014066 | 0.35 | 0.03 | enet | 35 | 0.07 | 1.2e-04 | 3.9 | 5.6 | 1.7e-08 | -0.25 | 0.24 | 0.08 | 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.