Table 2 Genotype frequencies comparison between cases and controls in the four SNPs tested, in both BC and MM pathologies

rs4516035

Codominant

CT

1.20 (0.92–1.56)

0.19

1.15 (0.83–1.58)

0.40

1.08 (0.73–1.60)

0.69

1.17 (0.70–1.96)

0.54

CC

1.16 (0.82–1.65)

0.41

0.97 (0.63–1.49)

0.88

1.51 (0.90–2.53)

0.12

1.79 (0.91–3.53)

0.09

Per minor allele

C-

1.09 (0.92–1.29)

0.30

1.01 (0.82–1.25)

0.91

1.20 (0.94–1.55)

0.15

1.31 (0.94–1.81)

0.11

rs2228570

Codominant

GA

1.14 (0.88–1.47)

0.32

1.26 (0.89–1.66)

0.22

1.09 (0.75–1.57)

0.66

1.23 (0.76–2.01)

0.40

AA

1.41 (0.96–2.08)

0.08

1.65 (1.02–2.65)

0.041

0.69 (0.38–1.25)

0.22

1.23 (0.55–2.73)

0.61

Per minor allele

A-

1.17 (0.98–1.40)

0.08

1.26 (1.02–1.57)

0.036

0.91 (0.70–1.19)

0.49

1.15 (0.81–1.64)

0.43

rs731236

Codominant

CT

0.84 (0.64–1.09)

0.19

0.82 (0.59–1.13)

0.22

1.26 (0.85–1.87)

0.25

1.06 (0.63–1.78)

0.81

CC

0.70 (0.50–0.98)

0.040

0.72 (0.48–1.09)

0.13

1.09 (0.64–1.84)

0.76

1.17 (0.57–2.39)

0.66

Per minor allele

C-

0.84 (0.71–0.99)

0.034

0.85 (0.69–1.03)

0.10

1.08 (0.84–1.40)

0.55

1.08 (0.77–1.52)

0.66

rs739837

Codominant

TG

0.96 (0.72–1.27)

0.76

0.96 (0.69–1.35)

0.83

0.89 (0.59–1.36)

0.60

0.64 (0.36–1.13)

0.12

GG

1.03 (0.74–1.44)

0.86

1.30 (0.87–1.96)

0.20

0.82 (0.50–1.36)

0.45

0.69 (0.35–1.38)

0.29

Per minor allele

G-

1.01 (0.86–1.20)

0.87

1.13 (0.92–1.38)

0.25

0.91 (0.71–1.17)

0.45

0.83 (0.59–1.16)

0.28