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GWAS Study

Genome-wide association study identifies multiple susceptibility loci for glioma.

Kinnersley B, Labussière M, Holroyd A et al.

26424050 PubMed ID
GWAS Study Type
12431 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

KB
Kinnersley B
LM
Labussière M
HA
Holroyd A
DS
Di Stefano AL
BP
Broderick P
VJ
Vijayakrishnan J
MK
Mokhtari K
DJ
Delattre JY
GK
Gousias K
SJ
Schramm J
SM
Schoemaker MJ
FS
Fleming SJ
HS
Herms S
HS
Heilmann S
SS
Schreiber S
WH
Wichmann HE
NM
Nöthen MM
SA
Swerdlow A
LM
Lathrop M
SM
Simon M
BM
Bondy M
SM
Sanson M
HR
Houlston RS
Chapter II

Abstract

Summary of the research findings

Previous genome-wide association studies (GWASs) have shown that common genetic variation contributes to the heritable risk of glioma. To identify new glioma susceptibility loci, we conducted a meta-analysis of four GWAS (totalling 4,147 cases and 7,435 controls), with imputation using 1000 Genomes and UK10K Project data as reference. After genotyping an additional 1,490 cases and 1,723 controls we identify new risk loci for glioblastoma (GBM) at 12q23.33 (rs3851634, near POLR3B, P=3.02 × 10(-9)) and non-GBM at 10q25.2 (rs11196067, near VTI1A, P=4.32 × 10(-8)), 11q23.2 (rs648044, near ZBTB16, P=6.26 × 10(-11)), 12q21.2 (rs12230172, P=7.53 × 10(-11)) and 15q24.2 (rs1801591, near ETFA, P=5.71 × 10(-9)). Our findings provide further insights into the genetic basis of the different glioma subtypes.

1,783 Northern European ancestry cases, 7,435 Northern European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

12431
Total Participants
GWAS
Study Type
Yes
Replicated
up to 1,490 European ancestry cases, up to 1,723 European ancestry controls
Replication Participants
European
Ancestry
U.S., Germany, U.K., France
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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Analysis In Progress

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