rs495828, None

N. diseases: 24
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.
Venous Thromboembolism
CUI: C1861172
Disease: Venous Thromboembolism
408 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 0.800 1.000 2 2011 2012
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 0.710 1.000 2 2018 2019
Hematocrit procedure
CUI: C0018935
Disease: Hematocrit procedure
216 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 0.700 1.000 2 2010 2017
Hemoglobin measurement
CUI: C0518015
Disease: Hemoglobin measurement
224 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 0.700 1.000 2 2010 2017
Red Blood Cell Count measurement
CUI: C0014772
Disease: Red Blood Cell Count measurement
1599 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 0.700 1.000 2 2010 2017
Alcohol consumption
CUI: C0001948
Disease: Alcohol consumption
535 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 0.700 1.000 1 2019 2019
Alkaline phosphatase measurement
CUI: C0201850
Disease: Alkaline phosphatase measurement
79 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 0.700 1.000 1 2010 2010
Blood Protein Measurement
CUI: C2985280
Disease: Blood Protein Measurement
2575 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 0.700 1.000 1 2019 2019
C-reactive protein measurement
CUI: C0201657
Disease: C-reactive protein measurement
624 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 0.700 1.000 1 2012 2012
Corpuscular Hemoglobin Concentration Mean
4389 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 0.700 1.000 1 2012 2012
Diabetes Mellitus, Non-Insulin-Dependent
2672 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 0.700 1.000 1 2013 2013
Eczema
CUI: C0013595
Disease: Eczema
368 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 0.700 1.000 1 2019 2019
Low density lipoprotein cholesterol measurement
1142 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 0.700 1.000 1 2019 2019
Protein measurement
CUI: C0202202
Disease: Protein measurement
422 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 0.700 1.000 1 2012 2012
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 0.700 1.000 1 2013 2013
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
1418 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 0.700 1.000 1 2019 2019
Venous Thrombosis
CUI: C0042487
Disease: Venous Thrombosis
218 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 0.700 1.000 1 2012 2012
von Willebrand's factor (lab test)
CUI: C2239219
Disease: von Willebrand's factor (lab test)
427 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 0.700 1.000 1 2013 2013
Coughing
CUI: C0010200
Disease: Coughing
16 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 0.020 1.000 2 2011 2014
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
293 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 0.010 1.000 1 2014 2014
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 0.010 1.000 1 2012 2012
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 0.010 1.000 1 2014 2014
Paroxysmal nocturnal hemoglobinuria
CUI: C0024790
Disease: Paroxysmal nocturnal hemoglobinuria
12 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 0.010 1.000 1 2017 2017
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 0.010 1.000 1 2014 2014