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. 2013 Mar 28;9(3):e1003419. doi: 10.1371/journal.pgen.1003419

Table 3. The Most Significant Associations of Each Gene's Burden of Coding Variants with Breast Cancer Risk.

Gene Chr # of SNPs OR P
Overall breast cancer, functional SNPs
MMAB 12 8 1.14 0.0000497
SLC16A6 17 6 1.10 0.0000541
INS-IGF2 11 4 0.88 0.000124
ST3GAL3 1 9 1.14 0.00016
SPDEF 6 14 1.10 0.000162
Overall breast cancer, rare SNPs
FGFBP3 10 5 26.6 0.00000871
LDLRAD1 1 10 1.63 0.0000209
NAALADL1 11 36 0.54 0.000147
UCHL1 4 2 11.17 0.000162
TXN2 22 2 3.03 0.000182
ER+ breast cancer, functional SNPs
SNTN 3 3 1.76 0.0000325
TXN2 22 2 3.74 0.0000373
SPATA16 3 20 0.93 0.0000505
APOC3 11 3 3.26 0.000257
APOC4 19 6 0.85 0.000266
ER+ breast cancer, rare SNPs
FGFBP3 10 5 35.35 0.000000621
LTBP4 19 33 0.53 0.0000199
TXN2 22 2 3.74 0.0000373
OR6C65 12 4 2.44 0.0000871
PRC1 15 13 2.02 0.000202
ER- breast cancer, functional SNPs
EGR2 10 4 32.27 0.0000000000124
CNR1 6 2 36.51 0.000000000168
MMAB 12 8 1.37 0.0000204
ATP6V1H 8 11 3.24 0.0000209
MRPL20 1 3 5.65 0.0000636
ER- breast cancer, rare SNPs
EGR2 10 4 32.27 0.0000000000124
CNR1 6 2 36.51 0.000000000168
FKSG83 6 5 4.40 0.0000000146
GATM 15 6 16.18 0.000000483
ACSBG1 15 11 2.63 0.000000533