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Table 3 Association between SNPs rs67311347, ATM rs1800057 and ALDH9A1 rs3845536 and risk of RCC

From: Association of single nucleotide polymorphisms with renal cell carcinoma in Algerian population

Polymorphisms Cases n % Controls n % Pa OR (95% CI)a Pa
rs67311347
 GG (ref) 29 (33.33%) 49 (42.98%)    
 GA 44 (50.57%) 57 (50.00%) 0.08 1.30 (0.71–2.38) 0.44
 AA 14 (16.09%) 8 (7.02%)   2.95 (1.10–7.89) 0.03
 G allele (ref) 102 (58.62%) 155 (67.98%)    
 A allele 72 (41.38%) 73 (32.02%)   1.49 (0.99–2.25) 0.05
ATM rs1800057
 CC (ref) 80 (91.95%) 113 (99.00%)    
 CG 6 (6.90%) 1 (0.88%) 0.03 8.47 (1.00–71.76) 0.04
 GG 1 (1.15%) 0 (0.00%)   Inf (Inf–Inf) 0.41
 C allele (ref) 166 (95.40%) 227 (100.00%)    
 G allele 8 (4.60%) 1 (0.44%)   10.93 (1.35–88.31) 0.01
ALDH9A1 rs3845536
 CC (ref) 35 (40.23%) 36 (32.43%)    
 CT 46 (52.87%) 51 (45.95%) 0.01 0.92 (0.50–1.71) 0.87
 TT 6 (6.90%) 24 (21.62%)   0.25 (0.09–0.70 0.007
 C allele 116 (66.67%) 123 (55.41%)    
 T allele 58 (33.33%) 99 (44.59%)   0.62 (0.41–0.93) 0.02
  1. aχ2 test or Fisher’s exact test. OR: Odds Ratio. CI: Confidence Interval