Gene-level analysis of rare variants in 379,066 whole exome sequences identifies an association of GIGYF1 loss of function with type 2 diabetes
Abstract Sequencing of large cohorts offers an unprecedented opportunity to identify rare genetic variants and to find novel contributors to human disease. We used gene-based collapsing tests to identify genes associated with glucose, HbA1c and type 2 diabetes (T2D) diagnosis in 379,066 exome-sequen...
Saved in:
Main Authors: | Aimee M. Deaton, Margaret M. Parker, Lucas D. Ward, Alexander O. Flynn-Carroll, Lucas BonDurant, Gregory Hinkle, Parsa Akbari, Luca A. Lotta, Regeneron Genetics Center, DiscovEHR Collaboration, Aris Baras, Paul Nioi |
---|---|
Format: | article |
Language: | EN |
Published: |
Nature Portfolio
2021
|
Subjects: | |
Online Access: | https://doaj.org/article/3eba2ec7d59241e2a1ea8ba7d9c77d4a |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
GWAS of serum ALT and AST reveals an association of SLC30A10 Thr95Ile with hypermanganesemia symptoms
by: Lucas D. Ward, et al.
Published: (2021) -
Acta Nº379
by: Banco Central de Chile
Published: (2019) -
GIGYF1 loss of function is associated with clonal mosaicism and adverse metabolic health
by: Yajie Zhao, et al.
Published: (2021) -
Translational repression of NMD targets by GIGYF2 and EIF4E2.
by: Boris Zinshteyn, et al.
Published: (2021) -
Ley Nº20.066. Establece Ley de Violencia Intrafamiliar
Published: (2005)