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. 2017 Dec 16;9(3):3677–3689. doi: 10.18632/oncotarget.23343

Table 2. Distribution of genotype/allele frequency of three SNPs in HOTAIR and their correlations with breast cancer.

Genotype Cases (n = 969) no.(%) Controls (n = 970) no.(%) P Adjusted OR
(95% CI)a
P trendb
rs1899663 G>T
GG 628 665 1.00 (Reference)
GT 299 284 0.326 1.11 (0.91–1.35)
TT 42 21 0.009 2.08 (1.20–3.60) 0.027
GT + TT 341 305 0.109 1.17 (0.97–1.42)
T allele frequency 383 (19.8) 326 (16.8) 0.017c
rs4759314 A>G
AA 801 817 1.00 (Reference)
GA 157 144 0.536 1.08 (0.84–1.39)
GG 11 9 0.805 1.12 (0.45–2.80) 0.520
GA + GG 168 153 0.514 1.08 (0.85–1.39)
A allele frequency 179 (9.2) 162 (8.4) 0.338c
rs7958904 G>C
GG 489 537 1.00 (Reference)
GC 396 373 0.171 1.14 (0.94–1.38)
CC 84 60 0.046 1.45 (1.01–2.08) 0.030
GC + CC 480 433 0.068 1.19 (0.99–1.42)
C allele frequency 564 (29.1) 493 (25.4) 0.010c

aAdjusted by age, BMI, age at menarche, menopausal status and family history of breast cancer where appropriate.

bP trend for genotypes between cases and controls.

cTwo-sided χ2 test for differences in allele frequency distributions between cases and cancer-free controls.