Common polymorphic transcript variation in human disease

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Figure 2.
Figure 2.

Examples of high-confidence transcript variant-genotype associations. For each gene, we show a subset of its exons (tall blue boxes indicate coding regions, shorter blue boxes indicate UTRs; transcription proceeds from left to right) in two known or predicted transcript variants, with (red bar) the location of the relevant probe set. (A–H, right panels) The data underlying each probe set's best genotype association.

This Article

  1. Genome Res. 19: 567-575

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