rs4912905, NR3C1

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.
Bodily Pain
CUI: C3890602
Disease: Bodily Pain
4 0.925 0.080 5 143350811 intron variant G/C snv 0.20 0.010 1.000 1 2015 2015
Infantile Spasm
CUI: C3887898
Disease: Infantile Spasm
39 0.925 0.080 5 143350811 intron variant G/C snv 0.20 0.010 1.000 1 2012 2012
West Syndrome
CUI: C0037769
Disease: West Syndrome
28 0.925 0.080 5 143350811 intron variant G/C snv 0.20 0.010 1.000 1 2012 2012