Table 2B.
Gene | Coverage (at r2 ≥ 0.8) |
Endometrioid (n = 2148)
|
Clear cell (n = 1013)
|
||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
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 | 2 | 0.47 | chr2:158719453:D | 0.06 | 0.85 | 1.14 | 0.042 | 0 | 0.87 | N/A | – | – | – | – |
ACVR2 | 0.98 | 1 | 0.25 | rs17742573 | 0.07 | 0.56 | 0.84 | 0.045 | 12 | 0.21 | rs55816333 | 0.42 | 0.97 | 0.89 | 0.018 |
CGA | 0.97 | 0 | 0.95 | N/A | – | – | – | – | 0 | 0.58 | N/A | – | – | – | – |
FSHB | 0.99 | 27 | 0.063 | rs7951733 | 0.08 | 0.95 | 0.76 | 4.62 × 10-5 | 0 | 0.46 | N/A | – | – | – | – |
FSHR | 0.90 | 19 | 0.34 | rs191446440 | 0.05 | 0.62 | 1.30 | 0.002 | 45 | 0.20 | rs55926033 | 0.12 | 0.87 | 1.21 | 0.007 |
GNRH | 1.00 | 0 | 0.13 | N/A | – | – | – | – | 1 | 0.35 | chr8:25290793:D | 0.09 | 0.55 | 1.23 | 0.038 |
GNRHR | 0.94 | 2 | 0.53 | rs148964181 | 0.13 | 0.55 | 1.12 | 0.045 | 3 | 0.31 | rs17637021 | 0.17 | 0.52 | 1.18 | 0.026 |
INHA | 0.86 | 3 | 0.14 | rs6436158 | 0.40 | 0.52 | 0.91 | 0.042 | 0 | 0.86 | N/A | – | – | – | – |
INHBA | 1.00 | 0 | 0.58 | N/A | – | – | – | – | 0 | 0.94 | N/A | – | – | – | – |
INHBB | 0.82 | 15 | 0.16 | rs12475606 | 0.47 | 0.55 | 0.90 | 0.016 | 2 | 0.70 | rs4528762 | 0.26 | 0.60 | 0.81 | 0.003 |
LHCGR | 0.97 | 8 | 0.65 | rs4293599 | 0.20 | 1.00 | 1.12 | 0.005 | 9 | 0.69 | rs3884614 | 0.07 | 0.66 | 1.29 | 0.005 |
Global | – | 77 | 0.33 | – | – | – | – | – | 72 | 0.53 | – | – | – | – | – |
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.