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Studies document extent to which common and rare genetic variants work in concert to shape blood traits and disease risk

In people with a single-gene variant that puts them at high risk for heart disease, breast cancer, or colorectal cancer, the rest of the genome can alter that risk.

COVID-19 test insights, an expanded elemental encyclopedia, where food choice and genetics meet, and more.

Pooled screening in human cells and molecular understanding of Huntington’s disease and pediatric brain cancers. 

Analyses of the largest publicly available catalog of human genomic data reveal new details on rare types of genetic variation and provide better tools for genetic disease diagnosis and drug development.

Analyzing cardiac measurements from large biobanks can uncover genetic predisposition to diseases like heart failure and arrhythmias.

Common in Peru but absent from European genomes, the variant may confer adaptive evolutionary advantage to populations who carry it

Genetic, geographic, and demographic data from more than 30,000 Americans reveal more genetic diversity within ancestry groups than previously thought.