Download rare variant results:
AoU_v6-noncoding-rare-genecentric_09-25-2023_SH_AKM.csv
AoU_v6-noncoding-rare-genecentric_no_tfbs_09-25-2023_SH_AKM.csv
AoU_v6-noncoding-rare-hubcentric_09-25-2023_SH.csv
AoU_v6-noncoding-rare-regulomecentric_09-25-2023_SH_AKM.csv
Publications
Rare Non-coding Variation Identified by Large Scale Whole Genome Sequencing Reveals Unexplained Heritability of Type 2 Diabetes.
Wessel J, et al.
medRxiv preprint
Phenotypes
- Type 2 diabetes (T2D)
Experiment summary
This study was a trans-ancestry meta-analysis of genetic associations for type 2 diabetes, based on whole-genome sequencing, in 25,760 participants in the All of Us study (9,812 cases and 15,948 controls).
Dataset ID
Wessel2024_T2D_AllOfUs_Mixed