Best TWAS P=9.617847e-08 · Best GWAS P=1.861017e-07 conditioned to 0.2919032
# | 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 | Sec31a | isoform ratio | ENSRNOT00000097169 | 0.05 | 0.02 | blup | 3203 | 0.03 | 7.9e-04 | 5.0 | 5.3 | 1.0e-07 | -0.94 | 0.35 | 0.63 | FALSE |
2 | Brain | Lin54 | alternative TSS | ENSRNOT00000003006 | 0.03 | 0.02 | lasso | 2 | 0.02 | 1.2e-02 | -5.2 | -5.2 | 1.9e-07 | 0.96 | 0.31 | 0.59 | FALSE |
3 | Brain | Lin54 | alternative TSS | ENSRNOT00000003006 | 0.04 | 0.02 | blup | 3225 | 0.03 | 1.5e-03 | -5.2 | -5.2 | 2.5e-07 | 0.87 | 0.30 | 0.67 | FALSE |
4 | Brain | Cops4 | gene expression | ENSRNOG00000023650 | 0.15 | 0.10 | enet | 17 | 0.15 | 1.9e-13 | -5.2 | -5.2 | 2.5e-07 | 0.78 | 0.27 | 0.73 | FALSE |
5 | Eye | Tmem150c | gene expression | ENSRNOG00000002258 | 0.31 | 0.10 | blup | 3691 | 0.15 | 2.9e-03 | 4.9 | 5.2 | 2.0e-07 | -0.89 | 0.41 | 0.34 | FALSE |
6 | LHb | Coq2 | gene expression | ENSRNOG00000002194 | 0.24 | 0.08 | top1 | 1 | 0.08 | 6.3e-03 | 5.1 | -5.1 | 2.9e-07 | 0.90 | 0.17 | 0.06 | FALSE |
7 | NAcc2 | Plac8 | gene expression | ENSRNOG00000002217 | 0.13 | 0.07 | blup | 3311 | 0.08 | 3.0e-05 | -4.7 | 5.1 | 2.9e-07 | -0.91 | 0.35 | 0.65 | FALSE |
8 | NAcc2 | Cops4 | gene expression | ENSRNOG00000023650 | 0.06 | 0.01 | blup | 3306 | 0.02 | 3.4e-02 | 4.5 | -5.3 | 1.5e-07 | 0.86 | 0.36 | 0.29 | FALSE |
9 | NAcc2 | Lin54 | mRNA stability | ENSRNOG00000002203 | 0.07 | 0.02 | blup | 3225 | 0.04 | 2.0e-03 | -4.8 | -5.3 | 9.6e-08 | 0.89 | 0.37 | 0.51 | TRUE |
10 | OFC | Hpse | gene expression | ENSRNOG00000002188 | 0.21 | 0.17 | top1 | 1 | 0.17 | 7.0e-05 | 5.1 | 5.1 | 2.9e-07 | -0.90 | 0.17 | 0.07 | 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.