rs1020397, ARNT2

N. diseases: 3
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Cryptorchidism
CUI: C0010417
Disease: Cryptorchidism
80 0.882 0.160 15 80426396 intron variant G/C;T snv 0.010 1.000 1 2012 2012
Hypospadias
CUI: C0848558
Disease: Hypospadias
80 0.882 0.160 15 80426396 intron variant G/C;T snv 0.010 1.000 1 2012 2012
Penile hypospadias
CUI: C1691215
Disease: Penile hypospadias
83 0.882 0.160 15 80426396 intron variant G/C;T snv 0.010 1.000 1 2012 2012