rs33389, NR3C1

N. diseases: 4
Source: BEFREE ×
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.
Anemia, Sickle Cell
CUI: C0002895
Disease: Anemia, Sickle Cell
68 0.882 0.280 5 143320934 intron variant C/G;T snv 0.010 1.000 1 2018 2018
Nephrotic Syndrome
CUI: C0027726
Disease: Nephrotic Syndrome
24 0.882 0.280 5 143320934 intron variant C/G;T snv 0.010 1.000 1 2008 2008
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
676 0.882 0.280 5 143320934 intron variant C/G;T snv 0.010 1.000 1 2009 2009
Steroid-sensitive nephrotic syndrome
CUI: C0403396
Disease: Steroid-sensitive nephrotic syndrome
11 0.882 0.280 5 143320934 intron variant C/G;T snv 0.010 1.000 1 2008 2008