Imputed data did not show any SNPs with substantially more significant associations with ovarian cancer risk except for rs3093926 in PARP2, associated with ovarian cancer risk in BRCA2 mutation carriers for which there was a SNP, rs61995542, with a stronger association (HR: 0.67, p = 4.6×10−4) (Figure S1). This evidence concerns the gene PARP2 and ovarian carcinoma.