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. 2020 Aug 24;4(11):bvaa121. doi: 10.1210/jendso/bvaa121

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© The Author(s) 2020. Published by Oxford University Press on behalf of the Endocrine Society.

This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com

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Figure 1. — Regional association plot of the type 2 diabetes association at chromosome 6p21.33 (location of coiled-coil α-helical rod protein 1 [CCHCR1]). Single-nucleotide variations (SNVs, formerly single-nucleotide polymorphisms [SNPs]) are plotted by position on chromosome 6 (x-axis) against association with type 2 diabetes from DIAMANTE (–log10 P value). The strongest signal at SNV rs3131012 is denoted by the purple diamond. Other SNVs are color-coded to reflect their linkage disequilibrium with the top SNV. The location and the direction of transcription for genes in the region are shown below the x-axis.