Figure 1

Figure 1. Coding variants in COL28A1 in DN patients from the Joslin Study on the Genetics of Type 2 Diabetes collection. From: The Genetic Risk of Kidney Disease in Type 2 Diabetes.

Ten variants identified in COL28A1’s coding sequence are shown, including 8 non-synonymous SNPs (red) and 2 synonymous SNPs (black). The rs identification numbers for variants reported in dbSNP build 135 are provided. Variants not in dbSNP build 135 are identified by their chromosome and position relative to NCBI Build 36.1.

Marcus G. Pezzolesi, et al. Med Clin North Am. ;97(1):91-107.

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