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A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21
Authors:van Heel David A  Franke Lude  Hunt Karen A  Gwilliam Rhian  Zhernakova Alexandra  Inouye Mike  Wapenaar Martin C  Barnardo Martin C N M  Bethel Graeme  Holmes Geoffrey K T  Feighery Con  Jewell Derek  Kelleher Dermot  Kumar Parveen  Travis Simon  Walters Julian R F  Sanders David S  Howdle Peter  Swift Jill  Playford Raymond J  McLaren William M  Mearin M Luisa  Mulder Chris J  McManus Ross  McGinnis Ralph  Cardon Lon R  Deloukas Panos  Wijmenga Cisca
Institution:Centre for Gastroenterology, Institute of Cell and Molecular Science, Queen Mary University of London, London E1 2AT, UK. d.vanheel@qmul.ac.uk
Abstract:We tested 310,605 SNPs for association in 778 individuals with celiac disease and 1,422 controls. Outside the HLA region, the most significant finding (rs13119723; P = 2.0 x 10(-7)) was in the KIAA1109-TENR-IL2-IL21 linkage disequilibrium block. We independently confirmed association in two further collections (strongest association at rs6822844, 24 kb 5' of IL21; meta-analysis P = 1.3 x 10(-14), odds ratio = 0.63), suggesting that genetic variation in this region predisposes to celiac disease.
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