Table 5.

Associations between genotypic frequencies of RAD51/G135C and types of chromosome alterations

	RAD51/G135C			P value GG × GC	P value GG × CC	P value GG × CC + GC
	GG	GC	CC
Translocations
0	58 (85.3%)	26 (68.4%)	6 (75.0%)	0.133	0.769	0.126
1	6 (8.8%)	7 (18.4%)	1 (12.5%)
2	3 (4.4%)	4 (10.5%)	1 (12.5%)
4	0 (0.0%)	1 (2.6%)	0 (0.0%)
5	1 (1.5%)	0 (0%)	0 (0.0%)
Chr. fragments
0	64 (94.0%)	30 (78.9%)	8 (100.0%)	0.004	1.000	0.014
1	2 (2.9%)	8 (21.1%)	0 (0.0%)
2	1 (1.5%)	0 (0%)	0 (0.0%)
3	1 (1.5%)	0 (0%)	0 (0.0%)
Chr. Breaks
0	63 (94.0%)	35 (92.1%)	6 (75.0%)	0.787	0.013	0.245
1	3 (4.5%)	3 (7.9%)	0 (0.0%)
2	0 (0.0%)	0 (0.0%)	2 (25.0%)
3	1 (1.5%)	0 (0.0%)	0 (0.0%)
Deletions
0	62 (91.2%)	34 (91.9%)	6 (75.0%)	0.731	0.197	0.774
1	4 (5.9%)	3 (8.1%)	1 (12.5%)
2	2 (2.9%)	0 (0.0%)	1 (12.5%)
Chr. Derivatives
0	65 (95.6%)	37 (97.4%)	8 (100.0%)	0.785	1.000	0.764
1	1 (1.5%)	1 (2.6%)	0 (0.0%)
2	2 (2.9%)	0 (0.0%)	0 (0.0%)
Inversions
0	68 (100.0%)	36 (97.3%)	8 (100.0%)	0.352	1.000	0.398
1	0 (0.0%)	1 (2.7%)	0 (0.0%)
Monosomies
0	62 (91.2%)	36 (94.7%)	6 (75.0%)	1.000	0.248	1.000
1	4 (5.9%)	2 (5.3%)	1 (12.5%)
2	1 (1.5%)	0 (0.0%)	1 (12.5%)
5	1 (1.5%)	0 (0.0%)	0 (0.0%)
Trisomies
0	67 (98.5%)	37 (97.4%)	8 (100.0%)	1.000	1.000	1.000
1	1 (1.5%)	1 (2.6%)	0 (0.0%)

P value < 0.05 was considered significant

Descriptive measures: a (± b), a = average and b = standard deviation