Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2241766
rs2241766 		0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		Cardiovascular Diseases 0.080 0.875 8 2005 2019
dbSNP: rs2241766
rs2241766 		0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.080 0.750 8 2006 2019
dbSNP: rs1501299
rs1501299 		0.597 0.720 3 186853334 intron variant G/C;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.070 1.000 7 2012 2018
dbSNP: rs2241766
rs2241766 		0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.060 1.000 6 2010 2018
dbSNP: rs266729
rs266729 		0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.060 0.833 6 2011 2019
dbSNP: rs1501299
rs1501299 		0.597 0.720 3 186853334 intron variant G/C;T snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.050 0.800 5 2011 2019
dbSNP: rs1501299
rs1501299 		0.597 0.720 3 186853334 intron variant G/C;T snv
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		Cardiovascular Diseases 0.050 0.600 5 2011 2018
dbSNP: rs2241766
rs2241766 		0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		Cardiovascular Diseases 0.040 1.000 4 2010 2018
dbSNP: rs266729
rs266729 		0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.040 1.000 4 2010 2017
dbSNP: rs1501299
rs1501299 		0.597 0.720 3 186853334 intron variant G/C;T snv
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		Cardiovascular Diseases 0.030 1.000 3 2012 2018
dbSNP: rs266729
rs266729 		0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		Cardiovascular Diseases 0.030 0.333 3 2011 2018
dbSNP: rs822395
rs822395 		0.776 0.240 3 186849018 intron variant C/A;G snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.030 1.000 3 2012 2019
dbSNP: rs1063537
rs1063537 		0.807 0.320 3 186856286 3 prime UTR variant C/T snv 9.6E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.020 1.000 2 2016 2018
dbSNP: rs266729
rs266729 		0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		Cardiovascular Diseases 0.020 1.000 2 2011 2011
dbSNP: rs266729
rs266729 		0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.020 1.000 2 2011 2012
dbSNP: rs12495941
rs12495941 		0.851 0.280 3 186850391 intron variant G/T snv 0.35
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.010 1.000 1 2018 2018
dbSNP: rs138227502
rs138227502 		0.925 0.040 3 186853221 missense variant C/T snv 1.8E-04 5.6E-04
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis 		Cardiovascular Diseases 0.010 1.000 1 2017 2017
dbSNP: rs138227502
rs138227502 		0.925 0.040 3 186853221 missense variant C/T snv 1.8E-04 5.6E-04
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis 		Cardiovascular Diseases 0.010 1.000 1 2017 2017
dbSNP: rs1501299
rs1501299 		0.597 0.720 3 186853334 intron variant G/C;T snv
CUI: C1704436
Disease: Peripheral Arterial Diseases
Peripheral Arterial Diseases 		Cardiovascular Diseases 0.010 1.000 1 2013 2013
dbSNP: rs17300539
rs17300539 		0.752 0.320 3 186841671 upstream gene variant G/A snv 5.3E-02
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.010 1.000 1 2017 2017
dbSNP: rs17366568
rs17366568 		0.851 0.200 3 186852664 non coding transcript exon variant G/A snv 8.8E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.010 1.000 1 2018 2018
dbSNP: rs17366743
rs17366743 		0.807 0.280 3 186854300 missense variant T/C snv 2.2E-02 2.1E-02
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		Cardiovascular Diseases 0.010 1.000 1 2019 2019
dbSNP: rs182052
rs182052 		0.701 0.440 3 186842993 intron variant G/A snv 0.38
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.010 1.000 1 2019 2019
dbSNP: rs182052
rs182052 		0.701 0.440 3 186842993 intron variant G/A snv 0.38
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.010 1.000 1 2019 2019
dbSNP: rs182052
rs182052 		0.701 0.440 3 186842993 intron variant G/A snv 0.38
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		Cardiovascular Diseases 0.010 1.000 1 2019 2019