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…de<->refseq. To fix this, before the cache is cleared and flagged variants are removed, keep track of flagged variants with interpretation and/or notes. Then after gene is analyzed, set the interpretation and notes on the matching variants. We will keep track of the user flagged state when the genome build changes, the gene source changes. Switching from advanced to basic/simple mode is more complicated as this reloads the entire app in the browser, so a separate issue (#1100) was created to address this problem.
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