As KCNQ1 was the gene in which most putative pathogenic SNVs were identified in the stillbirth cohort (n = 5), all missense and LoF variants recorded in ExAC NFE were systematically searched for in ClinVar, to get an approximation of how common pathogenic SNVs are in the European population for this gene. Here, KCNQ1 is linked to Stillbirth.