BRAVO — TOPMed

Variant browser providing allele frequencies for over 868 million variants from whole genomes.

What it does

Features deeply sequenced (>38X) WGS data, capturing ultra-rare variation that is routinely missed by standard exome cohorts.

How to use

See https://bravo.sph.umich.edu/ for documentation and access.

STRC usage

VERIFIED — E1659A NOT FOUND (404). Confirms variant rarity — absent from 868M variants in TOPMed deep WGS. Supports PM2.

Connections

• STRC Variant c.4976A>C — Misha [see-also]
• STRC Gene [about]
• [part-of] Tools index