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. Author manuscript; available in PMC: 2011 Apr 1.
Published in final edited form as: Circ Cardiovasc Genet. 2010 Feb 2;3(2):187–198. doi: 10.1161/CIRCGENETICS.109.904813

Figure 1A. Genetic variation at the human TH locus.

Figure 1A

LD blocks across the locus in 4 biogeographic ancestry groups. Common (minor allele frequency >10%) SNPs used to demonstrate LD (numbering from the ATG translational start codon): C-824T, G-801C, A-581G, G-494A, G1862A, G2066A, G2426C, G3034A, T3832C, C4581T, G4779A, C5162G, and T6681C. LD blocks were assigned by the solid spline method in Haploview. The TH exon/intron structure is superimposed above each panel; there were no common variants in the final (most 3′) exon.