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: rs2943634
rs2943634 		0.763 0.200 2 226203364 intergenic variant A/C;G snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.830 1.000 5 2007 2012
dbSNP: rs2943634
rs2943634 		0.763 0.200 2 226203364 intergenic variant A/C;G snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.750 1.000 6 2009 2018
dbSNP: rs2943634
rs2943634 		0.763 0.200 2 226203364 intergenic variant A/C;G snv
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.710 1.000 2 2012 2013
dbSNP: rs2943634
rs2943634 		0.763 0.200 2 226203364 intergenic variant A/C;G snv
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2943634
rs2943634 		0.763 0.200 2 226203364 intergenic variant A/C;G snv
CUI: C0578022
Disease: Finding of body mass index
Finding of body mass index 		0.700 1.000 1 2012 2012
dbSNP: rs2943634
rs2943634 		0.763 0.200 2 226203364 intergenic variant A/C;G snv
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2943634
rs2943634 		0.763 0.200 2 226203364 intergenic variant A/C;G snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2012 2012
dbSNP: rs2943634
rs2943634 		0.763 0.200 2 226203364 intergenic variant A/C;G snv
CUI: C0005893
Disease: Body mass index procedure
Body mass index procedure 		0.700 1.000 1 2012 2012
dbSNP: rs2943634
rs2943634 		0.763 0.200 2 226203364 intergenic variant A/C;G snv
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.030 1.000 3 2010 2012
dbSNP: rs2943634
rs2943634 		0.763 0.200 2 226203364 intergenic variant A/C;G snv
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis 		0.010 1.000 1 2013 2013
dbSNP: rs2943634
rs2943634 		0.763 0.200 2 226203364 intergenic variant A/C;G snv
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		0.010 1.000 1 2012 2012
dbSNP: rs2943634
rs2943634 		0.763 0.200 2 226203364 intergenic variant A/C;G snv
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		0.010 1.000 1 2012 2012
dbSNP: rs2943634
rs2943634 		0.763 0.200 2 226203364 intergenic variant A/C;G snv
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		0.010 1.000 1 2016 2016
dbSNP: rs2943634
rs2943634 		0.763 0.200 2 226203364 intergenic variant A/C;G snv
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		0.010 1.000 1 2012 2012
dbSNP: rs2943634
rs2943634 		0.763 0.200 2 226203364 intergenic variant A/C;G snv
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis 		0.010 1.000 1 2013 2013