Genome-wide association and multi-omics analyses provide insights into the disease mechanisms of central serous chorioretinopathy.

Among these 17 SNPs, the only one that was not located in a suggestive or genome-wide significant locus in the discovery meta-GWAS but showed a nominally significant association was rs10490924 at ARMS2 (effect allele/non-effect allele: T/G, Z-score = − 1.96, P = 0.050).

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