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. 2019 Jan 16;59(3):410–417. doi: 10.1111/head.13462

Table 2.

Genotype and Allele Frequencies for 3 HCRTR2 SNPs in Controls (n = 581) and CH Patients (n = 517)

Controls % (n) CH Patients % (n) χ2 (df) OR (95% CI) P Value P corr Value
rs3122156 Genotype TT 51.4 (298) 55.3 (286) 5.620 (2) .0602
TG 37.4 (217) 37.5 (194)
GG 11.2 (65) 7.2 (37)
Allele T 70.1 (813) 74.1 (766) 4.129 (1) 0.82 (0.68–0.99) .0421 .1263
G 29.9 (347) 25.9 (268)
rs2653342 Genotype GG 73.2 (424) 72.1 (373) 1.951 (2) .3770
GA 24.2 (140) 26.3 (136)
AA 2.6 (15) 1.5 (8)
Allele G 85.3 (988) 85.3 (882) 0.002 (1) 1.00 (0.79–1.27) .9622
A 14.7 (170) 14.7 (152)
rs2653349 Genotype GG 66.3 (385) 64.2 (332) 0.854 (2) .6525
GA 29.9 (174) 32.5 (168)
AA 3.8 (22) 3.3 (17)
Allele G 81.2 (944) 80.5 (832) 0.165 (1) 1.05 (0.85–1.30) .6843
A 18.8 (218) 19.5 (202)

χ2, chi‐square; CH, cluster headache; CI, confidence interval; df, degrees of freedom; OR, odds ratio; P corr value, P value corrected for multiple testing.