rs10733113, None

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.
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.882 0.160 1 247459055 upstream gene variant A/G snv 0.81 0.010 1.000 1 2009 2009
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.882 0.160 1 247459055 upstream gene variant A/G snv 0.81 0.010 1.000 1 2016 2016
Psoriasis vulgaris
CUI: C0263361
Disease: Psoriasis vulgaris
80 0.882 0.160 1 247459055 upstream gene variant A/G snv 0.81 0.010 1.000 1 2018 2018