Variant: rs121434272 

    present in Gene: PROK2
    present in Chromosome: 3
    Position on Chromosome: 71781472
    Alleles of this Variant: G/A;C

rs121434272 in PROK2 gene and HYPOGONADOTROPIC HYPOGONADISM 4 WITH OR WITHOUT ANOSMIA PMID 25077900 2014 The prevalence of CHD7 missense versus truncating mutations is higher in patients with Kallmann syndrome than in typical CHARGE patients.

PMID 23643382 2013 Mutations in FGF17, IL17RD, DUSP6, SPRY4, and FLRT3 are identified in individuals with congenital hypogonadotropic hypogonadism.

PMID 17054399 2006 Kallmann syndrome: mutations in the genes encoding prokineticin-2 and prokineticin receptor-2.

PMID 18559922 2008 Mutations in prokineticin 2 and prokineticin receptor 2 genes in human gonadotrophin-releasing hormone deficiency: molecular genetics and clinical spectrum.