rs200737258, AR

N. diseases: 4
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.
Chronic active hepatitis
CUI: C0520463
Disease: Chronic active hepatitis
34 0.882 0.240 X 67711476 missense variant G/A snv 2.1E-03 1.1E-03 0.010 1 2002 2002
Congenital adrenal hyperplasia
CUI: C0001627
Disease: Congenital adrenal hyperplasia
36 0.882 0.240 X 67711476 missense variant G/A snv 2.1E-03 1.1E-03 0.010 1.000 1 2002 2002
Congenital malformation of genital organs
CUI: C0158687
Disease: Congenital malformation of genital organs
1 0.882 0.240 X 67711476 missense variant G/A snv 2.1E-03 1.1E-03 0.010 1 2002 2002
Deficiency of steroid 21-monooxygenase
CUI: C0268287
Disease: Deficiency of steroid 21-monooxygenase
26 0.882 0.240 X 67711476 missense variant G/A snv 2.1E-03 1.1E-03 0.010 1.000 1 2002 2002