Abstract:
: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.
journal_name
Nat Communjournal_title
Nature communicationsauthors
Kinnersley B,Labussière M,Holroyd A,Di Stefano AL,Broderick P,Vijayakrishnan J,Mokhtari K,Delattre JY,Gousias K,Schramm J,Schoemaker MJ,Fleming SJ,Herms S,Heilmann S,Schreiber S,Wichmann HE,Nöthen MM,Swerdlow A,Lathrodoi
10.1038/ncomms9559subject
Has Abstractpub_date
2015-10-01 00:00:00pages
8559issn
2041-1723pii
ncomms9559journal_volume
6pub_type
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