Skip to main content
. Author manuscript; available in PMC: 2012 Jan 2.
Published in final edited form as: DNA Repair (Amst). 2010 Sep 15;10(1):111–116. doi: 10.1016/j.dnarep.2010.08.005

Table 2.

Main effects of 10 SNPs on melanoma risk in the additive model with P value ≤ 0.01

Gene SNP Wildtype Heterozygote Homozygous variant OR (95%CI)a P-trend

case/control case/control case/control
ATR rs13091637 115/150 80/58 15/1 2.20 (1.53–3.16) 0.00002
PARP1 rs3219125 169/189 43/16 1/0 3.13 (1.75–5.74) 0.0002
FANCA rs9926296 45/66 108/100 63/39 1.51 (1.15–1.99) 0.003
BLM rs8037430 117/88 80/94 14/29 0.64 (0.48–0.87) 0.004
MLH1 rs1540354 132/154 68/49 11/4 1.69 (1.16–2.47) 0.006
FANCA rs2239360 92/117 94/77 26/16 1.48 (1.11–1.98) 0.007
BLM rs7175811 100/75 94/106 16/31 0.67 (0.50–0.90) 0.008
PMS2 rs3779109 132/156 71/53 9/4 1.66 (1.13–2.43) 0.009
XRCC4 rs35268 162/141 47/63 4/10 0.59 (0.40–0.88) 0.009
XPG rs4150355 67/89 113/105 32/19 1.48 (1.10–2.00) 0.01
a

Adjusted by age.