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: rs1532624
rs1532624
0.851 0.160 16 56971567 intron variant C/A snv 0.34
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.700 1.000 1 2011 2011
dbSNP: rs1800775
rs1800775
0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.700 1.000 1 2011 2011
dbSNP: rs1864163
rs1864163
0.882 0.120 16 56963321 intron variant G/A snv 0.26
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.700 1.000 1 2011 2011
dbSNP: rs5882
rs5882
0.649 0.400 16 56982180 missense variant G/A;C snv 0.62
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.070 1.000 7 1998 2019
dbSNP: rs708272
rs708272
0.708 0.440 16 56962376 intron variant G/A snv 0.42 0.38
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.050 1.000 5 2014 2018
dbSNP: rs2303790
rs2303790
0.724 0.280 16 56983380 missense variant A/G snv 2.6E-03 6.5E-04
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.030 1.000 3 1996 2005
dbSNP: rs1800777
rs1800777
0.724 0.280 16 56983407 missense variant G/A snv 3.7E-02 2.8E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.020 0.500 2 2012 2014
dbSNP: rs4783961
rs4783961
0.851 0.320 16 56960982 upstream gene variant G/A snv 0.48 0.47
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.010 1.000 1 2018 2018
dbSNP: rs5880
rs5880
0.827 0.040 16 56981179 missense variant G/C snv 5.2E-02 3.7E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.010 1.000 1 2012 2012