Variant: rs606231407 

    present in Gene: LOC105378457;FGF8
    present in Chromosome: 10
    Position on Chromosome: 101770613
    Alleles of this Variant: C/T

rs606231407 in LOC105378457;FGF8 gene and Idiopathic hypogonadotropic hypogonadism PMID 23533228 2013 Prioritizing genetic testing in patients with Kallmann syndrome using clinical phenotypes.

rs606231407 in LOC105378457;FGF8 gene and Sense of smell impaired PMID 23533228 2013 Prioritizing genetic testing in patients with Kallmann syndrome using clinical phenotypes.