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: rs2107595
rs2107595 		0.732 0.280 7 19009765 regulatory region variant G/A snv 0.19
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		0.850 1.000 7 2012 2019
dbSNP: rs2107595
rs2107595 		0.732 0.280 7 19009765 regulatory region variant G/A snv 0.19
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.720 1.000 6 2015 2019
dbSNP: rs2107595
rs2107595 		0.732 0.280 7 19009765 regulatory region variant G/A snv 0.19
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		0.710 0.667 3 2015 2018
dbSNP: rs2107595
rs2107595 		0.732 0.280 7 19009765 regulatory region variant G/A snv 0.19
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.710 1.000 2 2014 2019
dbSNP: rs2107595
rs2107595 		0.732 0.280 7 19009765 regulatory region variant G/A snv 0.19
CUI: C0026654
Disease: Moyamoya Disease
Moyamoya Disease 		0.710 1.000 1 2018 2018
dbSNP: rs2107595
rs2107595 		0.732 0.280 7 19009765 regulatory region variant G/A snv 0.19
CUI: C2931384
Disease: Moyamoya disease 1
Moyamoya disease 1 		0.710 1.000 1 2018 2018
dbSNP: rs2107595
rs2107595 		0.732 0.280 7 19009765 regulatory region variant G/A snv 0.19
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 3 2017 2019
dbSNP: rs2107595
rs2107595 		0.732 0.280 7 19009765 regulatory region variant G/A snv 0.19
CUI: C1704436
Disease: Peripheral Arterial Diseases
Peripheral Arterial Diseases 		0.700 1.000 1 2019 2019
dbSNP: rs2107595
rs2107595 		0.732 0.280 7 19009765 regulatory region variant G/A snv 0.19
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		0.020 1.000 2 2016 2019
dbSNP: rs2107595
rs2107595 		0.732 0.280 7 19009765 regulatory region variant G/A snv 0.19
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis 		0.010 1.000 1 2019 2019
dbSNP: rs2107595
rs2107595 		0.732 0.280 7 19009765 regulatory region variant G/A snv 0.19
CUI: C0020473
Disease: Hyperlipidemia
Hyperlipidemia 		0.010 1.000 1 2016 2016
dbSNP: rs2107595
rs2107595 		0.732 0.280 7 19009765 regulatory region variant G/A snv 0.19
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis 		0.010 1.000 1 2019 2019
dbSNP: rs2107595
rs2107595 		0.732 0.280 7 19009765 regulatory region variant G/A snv 0.19
CUI: C0742343
Disease: Acute Chest Syndrome
Acute Chest Syndrome 		0.010 1.000 1 2016 2016
dbSNP: rs2107595
rs2107595 		0.732 0.280 7 19009765 regulatory region variant G/A snv 0.19
CUI: C4255010
Disease: Non-ST Elevated Myocardial Infarction
Non-ST Elevated Myocardial Infarction 		0.010 1.000 1 2016 2016
dbSNP: rs2107595
rs2107595 		0.732 0.280 7 19009765 regulatory region variant G/A snv 0.19
CUI: C1536220
Disease: ST segment elevation myocardial infarction
ST segment elevation myocardial infarction 		0.010 1.000 1 2016 2016