1471-2350-8-47-1.jpg (13.35 kB)
The structure of human gene drawn to an approximate scale
figure
posted on 2011-12-30, 18:49 authored by Katrin Kepp, Peeter Juhanson, Viktor Kozich, Mai Ots, Margus Viigimaa, Maris LaanCopyright information:
Taken from "Resequencing in European hypertensive and normotensive individuals: no common susceptibilily variants for hypertension and purifying selection on intron 1"
http://www.biomedcentral.com/1471-2350/8/47
BMC Medical Genetics 2007;8():47-47.
Published online 23 Jul 2007
PMCID:PMC1947951.
The identified SNPs (major allele by capital letters) are located relative to translation start site (ATG), where A denotes +1. SNPs with minor allele frequency 10% with long bars. Variants detected both in Estonians and Czech are shown in black; only in Czech are in grey and only in Estonians in white. The SNPs above and below the graph represent polymorphisms found in hypertensive and normotensive individuals, respectively. The 5'and 3'UTR have been indicated according to NCBI GenBank database (February 28, 2006 release).