Though the study was limited in ascertaining de novo from inherited variants, due to unavailability of paternal DNA, genes were reported by the authors that are either lethal, known to cause disease, or increase stillbirth risk (e.g., CCR5, FAT1, FLNB, INPP5K, MYO1C, PLOD2). The gene discussed is CCR5; the disease is Stillbirth.