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: rs1020397
rs1020397
0.882 0.160 15 80426396 intron variant G/C;T snv
CUI: C0010417
Disease: Cryptorchidism
Cryptorchidism
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Male Urogenital Diseases; Endocrine System Diseases 0.010 1.000 1 2012 2012
dbSNP: rs5000770
rs5000770
0.882 0.160 15 80424141 intron variant G/A snv 0.27
CUI: C0010417
Disease: Cryptorchidism
Cryptorchidism
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Male Urogenital Diseases; Endocrine System Diseases 0.010 1.000 1 2012 2012