New issue

Have a question about this project? Sign up for a free GitHub account to open an issue and contact its maintainers and the community.

Sign up for GitHub

By clicking “Sign up for GitHub”, you agree to our terms of service and privacy statement. We’ll occasionally send you account related emails.

Already on GitHub? Sign in to your account

Jump to bottom

[All] Add track for GnomAD / ClinVar #31

Open

jweile opened this issue Jul 26, 2018 · 0 comments

Labels

feature-request high-priority

Collaborator

jweile commented Jul 26, 2018

A track for variant effect maps showing where the Clinvar (likely)pathogenic, VUS and benign fall.

Maybe also for Gnomad rare (presumed non-pathogenic?; possibly filtered such that at least one homozygote has been seen).

jweile added the feature-request label

jweile added the high-priority label

Sign up for free to join this conversation on GitHub. Already have an account? Sign in to comment