Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs200895370
rs200895370
0.925 0.160 15 74417900 missense variant G/A;C snv 4.0E-04; 4.0E-06
Congenital hypogonadotropic hypogonadism
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Endocrine System Diseases 0.010 1.000 1 2014 2014
dbSNP: rs776572648
rs776572648
0.925 0.160 15 74411886 missense variant C/T snv 9.2E-05 5.6E-05
Congenital hypogonadotropic hypogonadism
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Endocrine System Diseases 0.010 1.000 1 2014 2014