Finally, at the OBFC1 locus, the strongest leiomyoma risk variant, rs7907606_G, has previously been associated with the risk of basal cell carcinoma25 and is strongly correlated with variants that have been reported for risk of melanoma26, adenocarcinoma of the lung27, thyroid cancer14, renal cell carcinoma24, serous ovarian cancer28, glioma29, and CLL30, as well as to telomere length31. The gene discussed is STN1; the disease is leiomyoma.