General report details for variant: ACMG criteria, GnomAD subpop info

Clinical-Genomics / scout

VCF visualization interface

https://clinical-genomics.github.io/scout

BSD 3-Clause "New" or "Revised" License

150 stars 46 forks source link

Open dnil opened 3 years ago

dnil commented 3 years ago

Especially on general report to speed up medical assessment - this apparently is one time thief when reading.

dnil commented 7 months ago

The GnomAD frequency should also always be displayed iff it exists, at least for all commented variants.