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Table 2 Allele (major) and genotype (major homozygote, heterozygote) frequencies for identified SNPs by resequencing in Estonian and Czech normotensives and hypertensives

From: Resequencing PNMTin European hypertensive and normotensive individuals: no common susceptibilily variants for hypertension and purifying selection on intron 1

SNPa dbSNP Alleleb/Genotype Estonians Czech
    Normotensives Hypertensives Normotensives Hypertensives
SNP-702 NA G 1 1 0.96 0.98
5'UTR   GG 1 1 0.92 0.96
   GA 0 0 0.08 0.04
SNP-591 NA G 0.96 0.96 0.98 0.88
5'UTR   GG 0.92 0.92 0.96 0.88
   GT 0.08 0.08 0.04 0
SNP-390 NA A 0.60 0.70 0.85 0.675
5'UTR   AA 0.44 0.40 0.79 0.45
   AG 0.32 0.60 0.125 0.45
SNP-184 rs876493 A 0.60 0.58 0.66 0.54
5'UTR   AA 0.40 0.24 0.44 0.20
   GA 0.40 0.68 0.44 0.68
SNP+360 rs200173 G 0.98 1 0.96 0.96
Intron 1   GG 0.96 1 0.92 0.92
   AG 0.04 0 0.08 0.08
SNP+1520 rs5638 A 0.94 0.96 0.94 0.96
Exon 3   AA 0.92 0.92 0.88 0.92
   AG 0.04 0.08 0.12 0.08
SNP+1587 NA G 0.98 1 1 0.98
Exon 3   GG 0.96 1 1 0.96
   AG 0.04 0 0 0.04
  1. alocation relative to ATG; bmajor allele frequency; NA-not available