Skip to main content
. Author manuscript; available in PMC: 2021 Oct 15.
Published in final edited form as: Nat Genet. 2020 Sep 14;52(10):1036–1045. doi: 10.1038/s41588-020-0684-4

Fig. 2 |. Genetic associations of the immune traits assessed.

Fig. 2 |

The innermost track shows the lowest association P value among all traits for each locus. Significant variants (P < 1.28 × 10−11) are in red, suggestive variants (P value ranging from 5 × 10−8 to 1.28 × 10−11) in orange, and non-significant variants in blue. The middle track shows the chromosome number. The outermost track indicates the genes nearest to signals with P < 1.28 × 10−11. Genes showing coincident genetic association with diseases are shown in bold font. The coincident associated genes are indicated even if in some instances their P values range from 5 × 10−8 to 1.28 × 10−11. The summary statistics were obtained using a linear mixed association model. The significance threshold was calculated by applying a Bonferroni correction to the empirical significance threshold (P = 6.9 × 10−9)6 considering 539 independent tests.