I have just realized that a GWAS that I ran sadly included related individuals (the flagged samples file that came with the dataset did not include relatedness). As relatedness is expected to increase false positives, is it reasonable to solely rerun the GWAS on the genome-significant hits, or do I need to rerun the entire analysis? We are mostly concerned about false positives with the results.
Does this answer your top level question or add additional information/context to it?
It should help control some bias and perhaps touch on related individuals, but I am seeking guidance/information from others.