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: rs495828
rs495828 		0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		0.800 1.000 1 2011 2012
dbSNP: rs495828
rs495828 		0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.710 1.000 1 2018 2019
dbSNP: rs495828
rs495828 		0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure 		0.700 1.000 2 2010 2017
dbSNP: rs495828
rs495828 		0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 2 2010 2017
dbSNP: rs495828
rs495828 		0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement 		0.700 1.000 2 2010 2017
dbSNP: rs495828
rs495828 		0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2019 2019
dbSNP: rs495828
rs495828 		0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2019 2019
dbSNP: rs495828
rs495828 		0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2019 2019
dbSNP: rs495828
rs495828 		0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81
CUI: C0013595
Disease: Eczema
Eczema 		0.700 1.000 1 2019 2019
dbSNP: rs495828
rs495828 		0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81
CUI: C0201850
Disease: Alkaline phosphatase measurement
Alkaline phosphatase measurement 		0.700 1.000 1 2010 2010
dbSNP: rs495828
rs495828 		0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 1.000 1 2019 2019