Data Snapshots
These aggregated, public-facing data snapshots provide an overview of All of Us Research Program participant characteristics and the types of data that we collect from participants.
Note: There are many stages of the All of Us participant journey. More than — people have registered with the program by creating online accounts at JoinAllofUs.org, beginning the enrollment process. The snapshots below highlight participants in the All of Us Research Program.
The following numbers are approximated to protect participants’ privacy. Numbers reflect data collected through —.
Participants at a Glance
—+
Participants
—+
Participants who have completed initial steps of the program
Enrollment Numbers
This graph represents participants who have consented to join the program and those who have completed all initial steps of the program. The initial steps are consenting, agreeing to share electronic health records, completing the first three surveys, providing physical measurements, and donating at least one biospecimen to be stored at the biobank.
The following numbers are approximated to protect participants’ privacy. Numbers are updated as of —.
100+
Funded Partner Organizations
—+
Sites Collecting Samples and Measurements
Outreach
These counts represent the number of program partner awardees and enrollment sites launched. These numbers are updated on an as-need basis.
Geography
This map reflects the number of participants in each state who have completed the initial steps of the program. The counts are updated daily. Note: Recruitment partners are located throughout the United States. Areas with a robust clinic presence will have a greater percentage of participants. As the program adds more sites and other ways to enroll, this map will become more uniform over time.
Diversity
Includes racial and ethnic minorities as well as sexual and gender minorities, people with low income or limited education, and other groups.
~45%
Racial and Ethnic Minorities
80+%
Underrepresented in Biomedical Research
Self-reported Categories
This graph represents the self-reported categories of participants who have completed the initial steps of the program. The information is based on participants’ responses to a question in The Basics survey. Each participant who answered this survey question is counted only once in the numbers below. Participants who selected more than one option are counted in “more than one category”.
Gender Identity
This graph represents the self-reported gender identities of participants who have completed the initial steps of the program. The information is based on participants’ responses to a question in the program’s The Basics survey. Because participants can select more than one option, the percentages in the graphs may not add up to 100%.
Age
This graph shows age at time of enrollment for participants who have completed the initial steps of the program. Age ranges are provided to protect participant privacy.
—+
Electronic Health Records
+
Biosamples
Please note: Data Browser counts may differ from Data Snapshots counts due to a delay between the time a participant consents and the time their record is included in the All of Us data that are visible in the Data Browser. Both datasets are considered valid by the All of Us Research Program for their intended purpose.
Dive into the Data
Use the interactive Data Browser to explore aggregate-level data derived from electronic health records, genomic sequencing, survey responses, physical measurements, and Fitbit activity.
The Data Browser is open to the public. No account or authorization is required.
