rs4795067, NOS2

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.
Psoriasis
CUI: C0033860
Disease: Psoriasis
705 0.882 0.280 17 27779649 intron variant A/G snv 0.31 0.820 1.000 5 2010 2015
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
243 0.882 0.280 17 27779649 intron variant A/G snv 0.31 0.010 1 2016 2016
Uveomeningoencephalitic Syndrome
CUI: C0042170
Disease: Uveomeningoencephalitic Syndrome
27 0.882 0.280 17 27779649 intron variant A/G snv 0.31 0.010 1 2016 2016