It was mind blowing: it identified 2 possible explanation that were already on my radar, 3 more that I had never considered of which one seems very likely and I am currently getting tested for, explained how each of those correlated with my symptoms and medical history, and asked why I had not had a specific marker tested (HLA b27) that is commonly checked for this type of disease (and indeed, my doctor was equally stumped - he just thought that test had been done already and didn't double-check).
Bonus: I asked if the specific marker could be inferred from whole genome sequencing data (had my genome sequenced last year). He told me which tool I could use, helped me align my sequencing data to the correct reference genome expected by that tool, gave me step by step instructions on how to prepare the data and tool, and I'm now waiting for results of the last step (NGS data analysis is veery slow).