Variant: rs121909665 

    present in Gene: FSHR
    present in Chromosome: 2
    Position on Chromosome: 48990629
    Alleles of this Variant: G/T

rs121909665 in FSHR gene and Ovarian Hyperstimulation Syndrome PMID 15080154 2004 A mutation in the follicle-stimulating hormone receptor as a cause of familial spontaneous ovarian hyperstimulation syndrome.

PMID 24058690 2013 Molecular analysis of a mutated FSH receptor detected in a patient with spontaneous ovarian hyperstimulation syndrome.

PMID 16278261 2006 Presence and absence of follicle-stimulating hormone receptor mutations provide some insights into spontaneous ovarian hyperstimulation syndrome physiopathology.

PMID 25581598 2015 Functional characterization of two naturally occurring mutations (Val514Ala and Ala575Val) in follicle-stimulating hormone receptor.

PMID 17721928 2008 Identification of the first germline mutation in the extracellular domain of the follitropin receptor responsible for spontaneous ovarian hyperstimulation syndrome.

PMID 12930928 2003 Ovarian hyperstimulation syndrome due to a mutation in the follicle-stimulating hormone receptor.

PMID 12930927 2003 A chorionic gonadotropin-sensitive mutation in the follicle-stimulating hormone receptor as a cause of familial gestational spontaneous ovarian hyperstimulation syndrome.