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首页> 外文期刊>Nature Genetics >Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants
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Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants

机译:对四种疾病中的14,500个非同义SNP进行关联扫描可确定自身免疫变异

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We have genotyped 14,436 nonsynonymous SNPs (nsSNPs) and 897 major histocompatibility complex (MHC) tag SNPs from 1,000 independent cases of ankylosing spondylitis ( AS), autoimmune thyroid disease (AITD), multiple sclerosis ( MS) and breast cancer ( BC). Comparing these data against a common control dataset derived from 1,500 randomly selected healthy British individuals, we report initial association and independent replication in a North American sample of two new loci related to ankylosing spondylitis, ARTS1 and IL23R, and confirmation of the previously reported association of AITD with TSHR and FCRL3. These findings, enabled in part by increased statistical power resulting from the expansion of the control reference group to include individuals from the other disease groups, highlight notable new possibilities for autoimmune regulation and suggest that IL23R may be a common susceptibility factor for the major `seronegative' diseases.
机译:我们已经对来自1,000例独立的强直性脊柱炎(AS),自身免疫性甲状腺疾病(AITD),多发性硬化症(MS)和乳腺癌(BC)的独立病例中的14,436个非同义SNP(nsSNPs)和897个主要组织相容性复合体(MHC)标签SNP进行了基因分型。将这些数据与从1500个随机选择的健康英国个体中得到的公共对照数据集进行比较,我们报告了北美样本中与强直性脊柱炎相关的两个新基因座ARTS1和IL23R的初始关联和独立复制,并证实了先前报道的与AITD与TSHR和FCRL3。这些发现在一定程度上是由于控制参考组扩大到包括其他疾病组的个体而导致的统计能力增强所致,这些发现突显了自身免疫调节的显着新可能性,并提示IL23R可能是主要的“血清阴性”的常见易感性因素。疾病。

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