Genome-wide significant association (p<1.×10<sup>−8</sup>) observed at the 11p11.2 locus.
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(a) SNPs for which no rsID has yet been allocated are named according to their position on chromosome 11. (b) Minor Allele Frequency. (c) P-value of the association between imputed SNPs and VT risk, after adjusting for principal components. (d) Imputation quality criterion (r2). (e) Combined meta-analysis p-value obtained using the Mantel-Haenszel inverse-variance weighting method.
创建时间：
2012-06-04
