Data Snapshots

Data Snapshots

The following collection of aggregated, public-facing data snapshots provides a quick overview of All of Us Research Program participant characteristics and information on the type of data collected from participants. Learn more about each snapshot by scrolling down below.

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 people who have completed enrollment, our participants.

The following numbers are approximated to protect participants’ privacy. Numbers are updated as of .

Participants at a Glance

+

Participants

+

Participants who have completed initial steps of the program

Enrollment Numbers

This graph represents participants (individuals who have consented to join the program) and participants who have completed all initial steps of the program (i.e., those who have consented, agreed to share their electronic health records, completed the first three surveys, provided physical measurements, and donated at least one biospecimen stored at the biobank).

The following numbers are approximated to protect participants’ privacy. Numbers are updated as of .

100+

Funded Partner Organizations

370+

Enrollment Sites Launched

Outreach

These counts represent the number of program partner awardees and enrollment sites launched. These numbers are updated on an as-need basis.

Geography

The count of participants represented in each state reflects the total number of participants who have completed the initial steps of the program. Each count is updated daily. Note: recruitment partners are located throughout the country. Areas with a robust clinic presence will have a greater percentage of participants; however, as the program adds more sites and other ways to enroll, this map will become more monochromatic 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. 

50%+

Racial and Ethnic Minorities

80%+

Underrepresented in Biomedical Research

Race & Ethnicity

This graph represents the self-reported races and ethnicities of participants who have completed the initial steps of the program, based on responses to “The Basics” survey. Each participant who answered this survey question is only counted once in the counts below. If a participant selected more than one option, they are counted in the “more than one race/ethnicity” category.

To learn more about this question, please visit “The Basics” in the Survey Explorer here.

Gender Identity

This graph represents the self-reported gender identities of participants who have completed the initial steps of the program, based on responses to “The Basics” survey. Because participants can select more than one option, the percentages in the graphs may not add up to 100%.

To learn more about this question, please visit “The Basics” in the Survey Explorer here.

Age

This graph represents the distribution of age for participants who have completed the initial steps of the program. Age ranges are provided to protect each participant’s privacy.

+

Electronic Health Records

+

Biosamples

Please note: The Snapshots dataset includes those recently enrolled and the latest All of Us Research Program updates. The Data Browser counts may differ from Data Snapshot counts due to a delay of several months between the time a participant consents and the time his/her record is included in the All of Us data that is visible in the Data Browser. The delay is a result of the time it takes for participant data to be collected, transferred to the Data and Research Center and curated. Both datasets are considered valid by the All of Us Research Program for their intended purpose. Please use the appropriate dataset when estimating the statistic of interest, as statistics may vary in the Snapshots and Data Browser datasets. When referencing these data, please name the dataset (Snapshots or Browser) and date the statistics were estimated.

Ready to Dive Into the Data?

DATA BROWSER

View public-facing aggregate data in our Data Browser. The includes information from surveys and physical measurements taken at the time of participant enrollment, as well as electronic health record data.

The Data Browser is open to all site visitors. No account or authorization is required.