Screening ‘test’ vs diagnostic ‘test’ is an important concept.
Screening tests are designed for sensitivity — false positives are expected and identify who would benefit from additional diagnostic tool and procedures.
Whole Genome Sequencing is affordable now. I’d suggest a 20x hifi long read from broad clinical labs for $1200 or so. Use opencravet to dig into the results. They just posted a webinar for personal analysis https://wse.zoom.us/webinar/register/WN_-VvYJ8FKRcGaKCQtLFrU...
Franklin by genoox is a slicker and possibly more approachable product depending on your interface preferences.
Genetic research — due to the number and subtly of variants — is ripe for citizen science in my opinion.
Screening tests are designed for sensitivity — false positives are expected and identify who would benefit from additional diagnostic tool and procedures.