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. Author manuscript; available in PMC: 2016 Oct 1.
Published in final edited form as: Gynecol Oncol. 2015 Aug 1;139(1):90–96. doi: 10.1016/j.ygyno.2015.07.110

Table 3.

Statistically significant associations between tag SNP's in the Th2 pathway and cervical and vulvar cancer risk, Seattle-Puget Sound Region, 1986-2004

Gene Site Cancer type SNP Function Allele Age-adjusted OR (95% CI) p-value
IL4R Vulva SCC (HPV+) rs3024668 nearGene-5 A/G 0.59(0.37,0.95) 0.0304
IL6 Cervix SCC (all subtypes) rs2069840 Intronic C/G 1.25(1.05,1.49) 0.0137
Cervix SCC (HPV16 only) rs2069840 Intronic C/G 1.32(1.02,1.70) 0.0327
rs2069837 Intronic A/G 0.42(0.21,0.81) 0.0101
IL10a Cervix SCC (HPV16 only) rs3024509 Intronic C/T 0.49(0.26,0.93) 0.0293
Cervix AC (HPV16 only) rs3024509 Intronic C/T 0.48(0.24,0.95) 0.0337
rs1800894 nearGene-5 A/G 0.34(0.12,0.94) 0.0376
IL10RAa,c Cervix AC (all subtypes) rs2229113b Missense A/G 1.21(1.02,1.43) 0.0304
rs2256111 coding sequence A/G 1.19(1.01,1.39) 0.0326
rs2512143 Intronic A/G 1.23(1.05,1.45) 0.0129
rs2512148 Intergenic A/C 1.22(1.04,1.44) 0.0172
IL10RBa Cervix AC (HPV16 only) rs2843701 Intronic C/T 0.75(0.57,0.98) 0.0327
TGFB1 Cervix SCC (all subtypes) rs11466338 Intronic A/G 1.48(1.05,2.09) 0.0243
TGFB2 Cervix SCC (HPV16 only) rs17047804 Intronic C/T 1.55(1.06,2.26) 0.0237
rs2000220 Intronic A/G 1.29(1.01,1.65) 0.0407
Cervix AC (all subtypes) rs4846476 Intronic C/G 0.81(0.67,0.99) 0.0396
TGFB3 Cervix SCC (all subtypes) rs3917148 Intronic A/C 1.36(1.00,1.85) 0.0494
Vulva SCC (HPV+) rs3917200 Intronic C/T 1.44(1.03,2.01) 0.0347
TGFBR1 Cervix SCC (all subtypes) rs10512263 Intronic C/T 0.66(0.46,0.94) 0.0226
Cervix SCC (HPV16 only) rs10512263 Intronic C/T 0.51(0.29,0.91) 0.0236
TGFBR2 Cervix AC (HPV16 only) rs9858487 Intronic C/G 1.69(1.00,2.83) 0.0481
Vulva SCC (HPV+) rs3087465 nearGene-5 A/G 1.23(1.00,1.51) 0.0451

Highlighted portions indicate previously published results from our study population.

a

Results for squamous cell carcinoma (all), adenocarconoma (all) and HPV+ vulvar cancer previously published by our group

b

rs2229113 had 5.1% missing genotype data

c

See reference 18 (Hussain et. al.)