rs1234314, TNFSF4

N. diseases: 7
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.
Systemic Scleroderma
CUI: C0036421
Disease: Systemic Scleroderma
287 0.790 0.320 1 173208253 upstream gene variant C/A;G snv 0.020 1.000 2 2010 2011
Lymphopenia
CUI: C0024312
Disease: Lymphopenia
16 0.790 0.320 1 173208253 upstream gene variant C/A;G snv 0.010 1.000 1 2013 2013
Allergic rhinitis (disorder)
CUI: C2607914
Disease: Allergic rhinitis (disorder)
176 0.790 0.320 1 173208253 upstream gene variant C/A;G snv 0.010 1.000 1 2017 2017
Acute Chest Syndrome
CUI: C0742343
Disease: Acute Chest Syndrome
135 0.790 0.320 1 173208253 upstream gene variant C/A;G snv 0.010 1.000 1 2019 2019
Acute Coronary Syndrome
CUI: C0948089
Disease: Acute Coronary Syndrome
139 0.790 0.320 1 173208253 upstream gene variant C/A;G snv 0.010 1.000 1 2019 2019
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.790 0.320 1 173208253 upstream gene variant C/A;G snv 0.010 1.000 1 2019 2019
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.790 0.320 1 173208253 upstream gene variant C/A;G snv 0.010 1.000 1 2019 2019