Source: GWASCAT

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: rs964184
rs964184
0.756 0.286 11 116778201 3 prime UTR variant G/C snp 0.83
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.810 1.000 3 2011 2016
dbSNP: rs964184
rs964184
0.756 0.286 11 116778201 3 prime UTR variant G/C snp 0.83
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.810 1.000 1 2012 2012
dbSNP: rs964184
rs964184
0.756 0.286 11 116778201 3 prime UTR variant G/C snp 0.83
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia
0.810 1.000 1 2010 2015
dbSNP: rs964184
rs964184
0.756 0.286 11 116778201 3 prime UTR variant G/C snp 0.83
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 10 2009 2017
dbSNP: rs964184
rs964184
0.756 0.286 11 116778201 3 prime UTR variant G/C snp 0.83
High density lipoprotein measurement
0.800 7 2009 2016
dbSNP: rs964184
rs964184
0.756 0.286 11 116778201 3 prime UTR variant G/C snp 0.83
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 6 2010 2017
dbSNP: rs964184
rs964184
0.756 0.286 11 116778201 3 prime UTR variant G/C snp 0.83
Low density lipoprotein cholesterol measurement
0.800 4 2010 2017
dbSNP: rs964184
rs964184
0.756 0.286 11 116778201 3 prime UTR variant G/C snp 0.83
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.800 1 2013 2013
dbSNP: rs964184
rs964184
0.756 0.286 11 116778201 3 prime UTR variant G/C snp 0.83
CUI: C1142098
Disease: Vitamin E Assay
Vitamin E Assay
0.800 1 2012 2012
dbSNP: rs964184
rs964184
0.756 0.286 11 116778201 3 prime UTR variant G/C snp 0.83
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.700 1 2016 2016
dbSNP: rs964184
rs964184
0.756 0.286 11 116778201 3 prime UTR variant G/C snp 0.83
Red cell distribution width determination
0.700 1 2017 2017
dbSNP: rs964184
rs964184
0.756 0.286 11 116778201 3 prime UTR variant G/C snp 0.83
CUI: C0578022
Disease: Finding of body mass index
Finding of body mass index
0.700 1 2016 2016
dbSNP: rs964184
rs964184
0.756 0.286 11 116778201 3 prime UTR variant G/C snp 0.83
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1 2016 2016
dbSNP: rs964184
rs964184
0.756 0.286 11 116778201 3 prime UTR variant G/C snp 0.83
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery
0.700 1 2012 2012
dbSNP: rs964184
rs964184
0.756 0.286 11 116778201 3 prime UTR variant G/C snp 0.83
CUI: C1318035
Disease: Platelet distribution width result
Platelet distribution width result
0.700 1 2017 2017
dbSNP: rs964184
rs964184
0.756 0.286 11 116778201 3 prime UTR variant G/C snp 0.83
Mean corpuscular hemoglobin concentration determination
0.700 1 2017 2017
dbSNP: rs964184
rs964184
0.756 0.286 11 116778201 3 prime UTR variant G/C snp 0.83
CUI: C0042879
Disease: Vitamin K Assay
Vitamin K Assay
0.700 1 2014 2014
dbSNP: rs964184
rs964184
0.756 0.286 11 116778201 3 prime UTR variant G/C snp 0.83
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.700 1 2016 2016
dbSNP: rs964184
rs964184
0.756 0.286 11 116778201 3 prime UTR variant G/C snp 0.83
CUI: C0337438
Disease: Glucose measurement
Glucose measurement
0.700 1 2016 2016
dbSNP: rs964184
rs964184
0.756 0.286 11 116778201 3 prime UTR variant G/C snp 0.83
Platelet distribution width measurement
0.700 1 2017 2017
dbSNP: rs964184
rs964184
0.756 0.286 11 116778201 3 prime UTR variant G/C snp 0.83
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation
0.700 1 2016 2016
dbSNP: rs964184
rs964184
0.756 0.286 11 116778201 3 prime UTR variant G/C snp 0.83
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure)
0.700 1 2017 2017
dbSNP: rs964184
rs964184
0.756 0.286 11 116778201 3 prime UTR variant G/C snp 0.83
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident
0.700 1 2016 2016
dbSNP: rs964184
rs964184
0.756 0.286 11 116778201 3 prime UTR variant G/C snp 0.83
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.700 1 2018 2018
dbSNP: rs964184
rs964184
0.756 0.286 11 116778201 3 prime UTR variant G/C snp 0.83
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.700 1 2016 2016