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: rs1883025
rs1883025
0.807 0.120 9 104902020 intron variant C/T snv 0.28
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.700 1.000 1 2011 2011
dbSNP: rs2515629
rs2515629
1.000 0.040 9 104832083 intron variant A/G snv 0.16
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.700 1.000 1 2011 2011
dbSNP: rs3890182
rs3890182
0.925 0.120 9 104885374 intron variant G/A;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.700 1.000 1 2011 2011
dbSNP: rs3905000
rs3905000
0.925 0.080 9 104894789 intron variant G/A snv 0.14
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.700 1.000 1 2011 2011
dbSNP: rs4149268
rs4149268
1.000 0.040 9 104884939 intron variant C/T snv 0.46
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.700 1.000 1 2011 2011
dbSNP: rs2230806
rs2230806
0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.100 0.917 12 2003 2019
dbSNP: rs4149313
rs4149313
0.763 0.240 9 104824472 missense variant T/C snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.030 1.000 3 2013 2019
dbSNP: rs1239681664
rs1239681664
0.716 0.320 9 104818690 synonymous variant A/G snv 7.0E-06
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.010 1.000 1 2014 2014
dbSNP: rs146292819
rs146292819
0.790 0.240 9 104794495 missense variant T/G snv 2.9E-04 3.8E-04
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.010 1.000 1 2019 2019
dbSNP: rs1800977
rs1800977
0.851 0.240 9 104928169 intron variant G/A;C snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.010 1.000 1 2019 2019
dbSNP: rs2066714
rs2066714
0.742 0.240 9 104824472 missense variant T/C snv 0.21 0.25
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.010 1.000 1 2006 2006
dbSNP: rs2066718
rs2066718
0.882 0.120 9 104826974 missense variant C/G;T snv 4.3E-04; 5.4E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.010 1.000 1 2006 2006
dbSNP: rs2740483
rs2740483
0.882 0.120 9 104928254 intron variant G/C snv 0.75
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.010 1.000 1 2016 2016
dbSNP: rs532997003
rs532997003
0.882 0.040 9 104840464 missense variant T/C snv 2.0E-05
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.010 1.000 1 2005 2005
dbSNP: rs9282541
rs9282541
0.790 0.160 9 104858554 missense variant G/A snv 1.3E-02 4.4E-03
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.010 1.000 1 2019 2019