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. 2004 Oct 18;101(43):15398–15403. doi: 10.1073/pnas.0404380101

Fig. 1.

Fig. 1.

Cumulative distributions of position-specific amino acid substitution scores for different sets of cSNPs. Distributions are shown for Mendelian disease (red), neutral variation (yellow), and “normal” human variation (green). The score distribution for complex diseases is in black squares. Shifts toward the left of the graph (smaller scores) indicate increasingly radical substitutions.