Table 2A.
Gene | Coverage (at r2 ≥ 0.8) |
Serous high grade (n = 6258)
|
Mucinous (n = 991)
|
||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
No. of signif. SNPs |
AML burden testb |
Most significant SNP |
MAFa | Imput. r2 |
ORc | p-Value | No. of signif. SNPs |
AML burden testb |
Most significant SNP |
MAFa | Imput. r2 |
ORc | p-Value | ||
ACVR1 | 0.55 | 0 | 0.47 | N/A | – | – | – | – | 1 | 0.76 | rs17804523 | 0.07 | 0.67 | 0.79 | 0.042 |
ACVR2 | 0.98 | 1 | 0.66 | rs57870939 | 0.05 | 0.60 | 1.13 | 0.038 | 6 | 0.38 | rs11681013 | 0.08 | 0.74 | 1.23 | 0.025 |
CGA | 0.97 | 0 | 0.69 | N/A | – | – | – | – | 1 | 0.50 | chr6:87820107:I | 0.29 | 0.89 | 1.11 | 0.039 |
FSHB | 0.99 | 1 | 0.35 | rs7925340 | 0.21 | 0.99 | 1.05 | 0.049 | 37 | 0.11 | rs12577729 | 0.22 | 0.95 | 1.14 | 0.018 |
FSHR | 0.90 | 31 | 0.52 | rs116044731 | 0.07 | 0.80 | 0.87 | 0.003 | 45 | 0.33 | rs12997920 | 0.39 | 0.88 | 1.13 | 0.010 |
GNRH | 1.00 | 12 | 0.041 | chr8:25283745:D | 0.42 | 0.62 | 1.07 | 0.010 | 0 | 0.40 | N/A | – | – | – | – |
GNRHR | 0.94 | 0 | 0.34 | N/A | – | – | – | – | 0 | 0.78 | N/A | – | – | – | – |
INHA | 0.86 | 5 | 0.24 | rs77120825 | 0.06 | 0.51 | 1.16 | 0.013 | 0 | 0.43 | N/A | – | – | – | – |
INHBA | 1.00 | 2 | 0.52 | rs17719440 | 0.08 | 0.98 | 1.11 | 0.008 | 0 | 0.55 | N/A | – | – | – | – |
INHBB | 0.82 | 12 | 0.15 | rs4328642 | 0.05 | 0.58 | 0.86 | 0.010 | 26 | 0.045 | rs6542591 | 0.39 | 0.67 | 1.17 | 0.003 |
LHCGR | 0.97 | 90 | 0.046 | rs13426172 | 0.12 | 1.00 | 0.91 | 0.005 | 21 | 0.67 | rs55871926 | 0.10 | 0.80 | 1.26 | 0.004 |
Global | – | 154 | 0.24 | – | – | – | – | – | 137 | 0.54 | – | – | – | – | – |
Note: “N/A” reflects genes with no significant SNPs at p ≥ 0.05. “Global” refers to when all genes are considered.
MAF = minor allele frequency.
AML = admixture maximum likelihood, taking into account the first five ancestry principal components; p-values for trend reported.
OR = per allele odds ratio, taking into account study set and the first five ancestry principal components.