Heterodox
Several years ago, I got my genome sequenced and obtained my variant call files, the tabulation of all differences between my gene sequences and the annotated human genome. Although my primary care physician was aware, I didn’t require his intermediation to obtain or interpret my genomics data. How I might react to adverse information was up to me. I’ve referred to my variant spreadsheet many times since then, whenever I’ve read about a new variant...
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