Logging in is optional. Signing in enables a few features:
Save variants and variant occurrences to return to them later from any device.
See searches you have run before, so you can quickly re-open a gene or variant you looked at earlier.
Vote on whether a variant has been correctly extracted from a paper. Votes are aggregated across users to surface the most reliable extractions. One vote per user per occurrence, which is why this requires login.
Leave comments on variant occurrences, e.g. to flag an incorrect extraction.
Searching for genes and variants, reading extracted variants and paper snippets, following links to UCSC / dbSNP / gnomAD, and subscribing to email updates work without an account.
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