Variant: rs587777863 

    present in Gene: PROK2;LOC105377156
    present in Chromosome: 3
    Position on Chromosome: 71784983
    Alleles of this Variant: C/G

rs587777863 in PROK2;LOC105377156 gene and HYPOGONADOTROPIC HYPOGONADISM 4 WITH OR WITHOUT ANOSMIA PMID 17054399 2006 Kallmann syndrome: mutations in the genes encoding prokineticin-2 and prokineticin receptor-2.

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