In FOXL2 (forkhead box L2), analysis of the exome of patient 1690 (South Asian), with 5 CHMs, 3 MCs, 1 stillbirth, and 1 live birth, identified a novel missense variant, NM_023067:c.500T>C, p.(Phe167Ser), in a homozygous state located in a run of homozygosity (ROH) of 10.5 Mb (Figure 1 and Supplemental Figure 1; supplemental material available online with this article; https://doi.org/10.1172/JCI170669DS1). This evidence concerns the gene FOXL2 and Stillbirth.