(a) Cumulative fraction of explained variance in disease liability (heritability) for each disease (see Methods). The loci are ordered from largest to smallest individual contribution. In total, 7.38, 10.30, 5.72, 2.53, and 5.95 percent of the heritability of ankylosing spondylitis (AS), Crohn's disease (CD), psoriasis (PS), primary sclerosing cholangitis (PSC) and ulcerative colitis (UC), respectively, is explained by the 169 loci outside the extended MHC region (for a maximum of 244 independent signals from ). When adding known risk alleles from the major histocompatibility complex (MHC)- to the 169 loci, the cumulative variance increases to 27.82, 10.88, 12.20, 5.48 and 7.66 percent for AS, CD, PS, PSC and UC, respectively.
(b) Example of a pair-wise comparison of heritability explained per risk variant between PS and UC. See for all ten pair-wise comparisons. Even if disease-associations account for approximately the same amount of variance explained in disease liability, e.g. as seen here for PS and UC, the pattern of sharing is complex in terms of size and direction of effect. Each box represents an independently associated SNP for the given disease. The size of each box is proportional to the amount of heritability for that variant. The colors of the boxes denote whether the difference in variance explained is due to different direction of effect (risk versus protective), significant heterogeneity of odds ratios (P<0.01) or both.