Menu
Currency
GWAS Study

Genetic architecture of type 1 diabetes with low genetic risk score informed by 41 unreported loci.

Qu HQ, Qu J, Bradfield J et al.

34302048 PubMed ID
GWAS Study Type
13280 Participants
78 Views
Scroll to explore
Chapter I

Publication Details

Comprehensive information about this research publication

Authors

QH
Qu HQ
QJ
Qu J
BJ
Bradfield J
ML
Marchand L
GJ
Glessner J
CX
Chang X
MM
March M
LJ
Li J
CJ
Connolly JJ
RJ
Roizen JD
SP
Sleiman P
PC
Polychronakos C
HH
Hakonarson H
Chapter II

Abstract

Summary of the research findings

Type 1 diabetes (T1D) patients with low genetic risk scores (GRS) may be non-autoimmune or autoimmune mediated by other genetic loci. The T1D-GRS2 provides us an opportunity to look into the genetic architecture of these patients. A total of 18,949 European individuals were included in this study, including 6599 T1D cases and 12,323 controls. 957 (14.5%) T1D patients were identified with low GRS (GRS < 8.43). The genome-wide association study on these patients identified 41 unreported loci. Two loci with common variants and 39 loci with rare variants were identified in this study. This study identified common SNPs associated with both low GRS T1D and expression levels of the interferon-α-induced MNDA gene, indicating the role of viral infection in T1D. Interestingly, 16 of the 41 unreported loci have been linked to autism spectrum disorder (ASD) by previous studies, suggesting that genes residing at these loci may underlie both T1D and autism.

957 European ancestry cases, 12,323 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

13280
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
Canada, U.S.
Recruitment Country
Chapter IV

AI-Generated Summary

AI-generated by DNAGENICS

Independent AI summary of health and genetic findings from the published study

Important: This summary is AI-generated by DNAGENICS for informational purposes only. It was not created by, affiliated with, or endorsed by the researchers behind the original publication, and is based solely on that published research. It may contain errors or omissions. DNAGENICS disclaims all liability for any inaccuracies or consequences arising from use of this information. Verify all information against the original publication. This is not professional scientific review or medical advice.

AI Summary In Progress

Our AI-generated summary of this publication is being prepared. Please check back soon.