Evidence map›Paper›PMID 42619260›Full record

ArticleHGG advances2026

The pleiotropic landscape of rare variant associations with multiple cancers in large biobanks.

Austin Hammermeister Suger, Tabitha A Harrison, Jiachen Zhang, Michael C Wu, Burcu F Darst, Sara Lindström

Abstract read
In one paragraph

Article in HGG advances, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Austin Hammermeister SugerDepartment of Epidemiology, University of Washington School of Public Health, 3980 15th Ave. NE, Seattle, WA 98195, USA. Electronic address: austinhammermeistersuger@gmail.com.
Tabitha A HarrisonDepartment of Epidemiology, University of Washington School of Public Health, 3980 15th Ave. NE, Seattle, WA 98195, USA.
Jiachen ZhangInstitute for Public Health Genetics, University of Washington School of Public Health, 1705 NE Pacific St., Seattle, WA 98195, USA.
Michael C WuPublic Health Sciences Division, Fred Hutchinson Cancer Center, 1100 Fairview Ave. N, Seattle, WA 98109, USA.
Burcu F DarstPublic Health Sciences Division, Fred Hutchinson Cancer Center, 1100 Fairview Ave. N, Seattle, WA 98109, USA.
Sara LindströmDepartment of Epidemiology, University of Washington School of Public Health, 3980 15th Ave. NE, Seattle, WA 98195, USA; Public Health Sciences Division, Fred Hutchinson Cancer Center, 1100 Fairview Ave. N, Seattle, WA 98109, USA.

Funding

Translational Bioimaging Core Shared ResourceP30CA015704 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Marian Esvelt · 1985 to 2026
$296.4M
TRANSCRIPTOME AND PROTEOME STRATIFICATION OF PROSTATE ADENOCARCINOMA PHENOTYPESP50CA097186 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI PETER S NELSON · 2002 to 2026
$58.1M
Developing Data-Driven Cancer ResearchersT32CA009168 · NCI · UNIVERSITY OF WASHINGTON · PI STEPHEN M SCHWARTZ, MICHAEL Chiao-An WU · 1985 to 2026
$10.1M
Quantifying and Characterizing the shared genetic contribution to common cancersU01CA194393 · NCI · UNIVERSITY OF WASHINGTON · PI KRAFT, PETER, LINDSTROEM, SARA · 2015 to 2023
$3.0M
Germline Genetics and Risk of Prostate Cancer in Diverse Populations from the All of Us ProgramR03CA287235 · NCI · FRED HUTCHINSON CANCER CENTER · PI DARST, BURCU FRANCES · 2023 to 2024
$368k
NCI NIH HHS P30 CA015704NCI NIH HHS P50 CA097186NCI NIH HHS R03 CA287235NCI NIH HHS T32 CA009168NCI NIH HHS U01 CA194393
6 · The paper itself

Abstract

Previous association studies between germline rare genetic variation and cancer risk have primarily examined a limited number of cancers in clinical samples, often with participants predominantly of European genetic ancestry. We conducted exome-wide rare variant association analyses across 70+ cancer types using data from more than 729,000 participants from the UK Biobank (UKB) and All of Us (AoU) Research Program cohorts. We used generalized linear mixed models to screen for cancer pleiotropic effects by conducting gene-based and single-variant tests of predicted loss of function (pLoF) and missense variants and six groups of cancer defined by biological and etiological similarities. We then assessed significant genes for associations with 27 individual cancer types that had data for at least 500 affected individuals. Of the 33 potential pleiotropic genes identified, 16 consistently showed significant associations across ≥3 individual cancer types. For example, the presence of at least one CHEK2 pLoF variant was associated with increased odds of diagnosis with 14 different cancers (odds ratio [OR] range: 1.34-3.21). Similarly, the presence of at least one RTEL1 missense variant was associated with lower odds of diagnosis with 9 cancers (OR range: 0.67-0.88). Our results expand our knowledge about these loci and point to a larger impact on overall cancer risk than previously appreciated.

Indexed as

biobanksexome sequencingmultiple cancerspleiotropyrare variants

Identifiers

PMID42619260
PMCPMC13571141

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.