Myriad Genetics at ASHG 2026

Oct 20–24, 2026 Montréal, Canada ~7.5k attendees Website

Myriad Genetics at ASHG 2026 in Montréal: 2 presentations (2 posters).

OrganizationASHG 2026 Attendance
Myriad Genetics
Salt Lake City, Utah
1 Lab Director · 1 other presenter
Public company~2,700 people
Myriad sells molecular diagnostic tests for hereditary cancer, oncology, and prenatal care. It serves patients, healthcare providers, and biopharma partners.
Myriad fully launched FirstGene, its Multiple Prenatal Screen, a new commercial test now broadly available.
›
Myriad fully launched FirstGene, its Multiple Prenatal Screen, a new commercial test now broadly available.
2026-07 · source
Myriad expanded Precise MRD availability to breast, colorectal, and renal cancer patients undergoing treatment and surveillance.
2026-06 · source
Myriad named Raj Jampa chief technology officer effective June 1, 2026, a new technical leadership contact.
2026-06 · source
Source: company newsroom
Q2 2026 revenue $190.7M, down 11%
›
FY2026 guidance is $770M-$790M revenue with 66%-67% adjusted gross margin, signaling a cautious outlook. · 2026-07-30
““Second quarter 2026 revenue of $190.7 million decreased 11% year-over-year”; “Revenue | $770 - $790”; “Adjusted Gross Margin % | 66% - 67%.””
Source: results release
Poster
Thu Oct 22
4:15 pm
Localization of Large Rearrangements in PMS2 and PMS2CL using PacBio
Cancer syndromesDiagnosticsGenetic testingLong-read sequencing
Poster
Fri Oct 23
2:30 pm

Explore the full ASHG 2026 dataset

Get in-depth attendee and institution profiles and research, to plan your meetings in Montréal. Leave your work email and we’ll be in touch.

Privacy

Download the full ASHG 2026 CSV

Leave your work email and we’ll be in touch. The CSV adds attendee names, roles and contact details to the company and session data shown here.

Privacy

Instantly find 20 buyers from Myriad Genetics

Get a list of who you should contact, their contact info, and what to say.

Totally free and instant, no sign up necessary!

Not affiliated with or endorsed by the American Society of Human Genetics. Submit a correction