We determined credible variants among the independent variants by merging risk variants within 1Mb of the lead variant and fine-mapped the resulting region with 95% credible sets using FINEMAP.90 Posterior inclusion probability ranges from 0 to 1 with values closer to 1 indicating greater causal probability. We implicated a putative causal variant if it accounted for > 50% of the posterior probability in the 95% credible set.
