Table 1

Genotype and allele frequencies of the A3669G SNP of GR in 499 patients with PMF and the healthy control populations

NGR A3669G genotype, no. (%)
Allele frequency, %
A/AA/GG/GA/G + G/GAG
PMF patients 499 274 (54.9) 188 (37.7) 37 (7.4) 225 (45.1)* 73.7 26.2 
Local controls 111 73 (65.7) 36 (32.4) 2 (1.8) 38 (34.2) 81.98 18.02 
WTCCC controls 2837 1997 (70.4) 763 (26.9) 77 (2.7) 840 (29.6) 83.8 16.2 
NGR A3669G genotype, no. (%)
Allele frequency, %
A/AA/GG/GA/G + G/GAG
PMF patients 499 274 (54.9) 188 (37.7) 37 (7.4) 225 (45.1)* 73.7 26.2 
Local controls 111 73 (65.7) 36 (32.4) 2 (1.8) 38 (34.2) 81.98 18.02 
WTCCC controls 2837 1997 (70.4) 763 (26.9) 77 (2.7) 840 (29.6) 83.8 16.2 
*

The A/G plus G/G genotype frequency was higher in patients with PMF with respect to local controls (P = .028) and WTCCC controls (P < .001)

The G allele frequency was statistically higher in PMF patients with respect to local controls (OR, 1.62; 95% CI, 1.12-2.35; P = .009) and WTCCC controls (OR, 1.84; 95% CI, 1.571-2.15; P < .001).

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