Genome-wide association study of follicular lymphoma identifies a risk locus at 6p21.32
Autoři | |
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Rok publikování | 2010 |
Druh | Článek v odborném periodiku |
Časopis / Zdroj | Nature genetics |
Fakulta / Pracoviště MU | |
Citace | |
Doi | http://dx.doi.org/10.1038/ng.626 |
Obor | Genetika a molekulární biologie |
Klíčová slova | NON-HODGKIN-LYMPHOMA; NECROSIS-FACTOR TNF; HIGH-RESOLUTION; HLA; SUSCEPTIBILITY; HAPLOTYPE; POLYMORPHISMS |
Popis | To identify susceptibility loci for non-Hodgkin lymphoma subtypes, we conducted a three-stage genome-wide association study. We identified two variants associated with follicular lymphoma at 6p21.32 (rs10484561, combined P = 1.12 x 10(-29) and rs7755224, combined P = 2.00 x 10(-19); r(2) = 1.0), supporting the idea that major histocompatibility complex genetic variation influences follicular lymphoma susceptibility. We also found confirmatory evidence of a previously reported association between chronic lymphocytic leukemia/small lymphocytic lymphoma and rs735665 (combined P = 4.24 x 10(-9)). |