Source: BEFREE

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: rs2066715
rs2066715
0.807 0.160 9 104825752 missense variant C/T snv 8.2E-02 5.5E-02
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis
0.010 < 0.001 1 2015 2015
dbSNP: rs2066715
rs2066715
0.807 0.160 9 104825752 missense variant C/T snv 8.2E-02 5.5E-02
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke
0.010 1.000 1 2019 2019
dbSNP: rs2066715
rs2066715
0.807 0.160 9 104825752 missense variant C/T snv 8.2E-02 5.5E-02
CUI: C0007785
Disease: Cerebral Infarction
Cerebral Infarction
0.010 1.000 1 2010 2010
dbSNP: rs2066715
rs2066715
0.807 0.160 9 104825752 missense variant C/T snv 8.2E-02 5.5E-02
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.010 < 0.001 1 2010 2010
dbSNP: rs2066715
rs2066715
0.807 0.160 9 104825752 missense variant C/T snv 8.2E-02 5.5E-02
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.010 1.000 1 2012 2012
dbSNP: rs2066715
rs2066715
0.807 0.160 9 104825752 missense variant C/T snv 8.2E-02 5.5E-02
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.010 1.000 1 2003 2003
dbSNP: rs2066715
rs2066715
0.807 0.160 9 104825752 missense variant C/T snv 8.2E-02 5.5E-02
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
0.010 < 0.001 1 2015 2015