Estimates of the explained variances in the twelve quantitative phenotypes attributable to chromosome X SNPs and autosomal SNPs separately using equal variance (EV) model.

The estimates are based on an analysis of the individuals from six Finnish cohorts using the program GCTA and 217,112 common and low-frequency chrX SNPs (MAF>1%) directly genotyped or imputed with high-quality (info >0.8) and 319,445 directly genotyped autosomal SNPs (MAF>1%).hX: estimate for the proportion of explained variance accountable by the SNPs in chromosome X in per cent; seX: standard error in per cent for the X chromosome variance estimate; P-value: P-value for the test of hX = 0; haut: estimate for the proportion of explained variance accountable by the SNPs in autosomes in per cent; seaut: standard error in per cent for the autosomal variance estimate; SBP: systolic blood pressure; HDL-C: high-density lipoprotein cholesterol; TG: total triglycerides; CRP: C-reactive protein; WHR: waist-hip-ratio; BMI: body-mass-index; DBP: diastolic blood pressure; LDL-C: low-density lipoprotein cholesterol; TC: total cholesterol.