GREB1L and Mayer-Rokitansky-Kuster-Hauser syndrome type 1: Several studies associated variants in GREB1L to congenital kidney malformations/agenesis [39–41], urogenital adysplasia, and Mayer-Rokitansky‐Kuster‐Hauser syndrome [13, 42] suggesting its role in the functioning of the urogenital systems.