Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C2747816
Disease: Complicated malaria
Complicated malaria
0.010 1.000 1 2007 2007
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0024535
Disease: Malaria, Falciparum
Malaria, Falciparum
0.010 1.000 1 2007 2007
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 2010 2010
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.010 1.000 1 2010 2010
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.010 1.000 1 2010 2010
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0553694
Disease: Oropharyngeal disorders
Oropharyngeal disorders
0.010 1.000 1 2010 2010
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 1 2010 2010
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0030193
Disease: Pain
Pain
0.010 1.000 1 2012 2012
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0549523
Disease: Oropharynx (excludes nasopharynx)
Oropharynx (excludes nasopharynx)
0.010 1.000 1 2013 2013
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0206081
Disease: Hyperandrogenism
Hyperandrogenism
0.010 1.000 1 2013 2013
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 2013 2013
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
Immune Reconstitution Inflammatory Syndrome
0.010 1.000 1 2013 2013
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C1096197
Disease: Immune reconstitution syndrome
Immune reconstitution syndrome
0.010 1.000 1 2013 2013
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C2607914
Disease: Allergic rhinitis (disorder)
Allergic rhinitis (disorder)
0.010 1.000 1 2013 2013
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome
0.020 1.000 2 2013 2014
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0030920
Disease: Peptic Ulcer
Peptic Ulcer
0.010 1.000 1 2014 2014
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0011311
Disease: Dengue Fever
Dengue Fever
0.020 1.000 2 2013 2015
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy
0.010 1.000 1 2015 2015
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0023343
Disease: Leprosy
Leprosy
0.010 1.000 1 2015 2015
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
Diabetes Mellitus, Non-Insulin-Dependent
0.010 1.000 1 2015 2015
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.010 1.000 1 2016 2016
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0742343
Disease: Acute Chest Syndrome
Acute Chest Syndrome
0.010 1.000 1 2016 2016
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0266929
Disease: Chronic Periodontitis
Chronic Periodontitis
0.010 1.000 1 2016 2016
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.010 1.000 1 2016 2016
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.010 1.000 1 2016 2016