Download rare variant results:
TOPMed_T2D_AdjBMI_smmat_gene_centric_0.01pct_2022Oct13_09-25-2023_SH.csv
TOPMed_T2D_AdjBMI_smmat_gene_centric_no_tfbs_0.01pct_2022Oct13_09-25-2023_SH.csv
TOPMed_T2D_AdjBMI_smmat_hub_centric_0.01pct_2022Oct13_09-25-2023_SH.csv
TOPMed_T2D_AdjBMI_smmat_regulomecentric_0.01pct_2022Oct13_09-25-2023_SH.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 59,633 participants in the TOPMed study (13,806 cases and 45,827 controls).
Dataset ID
Wessel2024_T2D_TOPMED_Mixed