<p>A discovery GWAS is performed, consisting of genotyping 221 Waldenstrom macroglobulinemia (WM) cases on the Illumina Omni Express 12v1.1 platform and analyzing the genotypes together with those of 3798 previously genotyped controls in a model taking into account gender, age, and principal components of ancestry (i.e., significant eigenvectors). Directly genotyped data are supplemented by imputation using the Haplotype Reference Consortium.</p>

NCI Waldenstrom Macroglobulinemia Genome-Wide Association Study

Waldenstrom Macroglobulinemia study with SNP Genotypes (Array), SNP Genotypes (imputed) data on dbGaP (217 participants)

NCI Waldenstrom Macroglobulinemia Genome-Wide Association Study

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