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.
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
243 0.925 0.200 7 129770387 non coding transcript exon variant C/G;T snv 5.9E-02 0.010 1.000 1 2014 2014
Glaucoma, Primary Open Angle
CUI: C0339573
Disease: Glaucoma, Primary Open Angle
222 0.925 0.200 7 129770387 non coding transcript exon variant C/G;T snv 5.9E-02 0.010 1.000 1 2016 2016
Late insomnia
CUI: C0581874
Disease: Late insomnia
1 0.925 0.200 7 129770387 non coding transcript exon variant C/G;T snv 5.9E-02 0.010 1.000 1 2010 2010
Sleeplessness
CUI: C0917801
Disease: Sleeplessness
30 0.925 0.200 7 129770387 non coding transcript exon variant C/G;T snv 5.9E-02 0.010 1.000 1 2010 2010