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: rs1333042
rs1333042
0.827 0.120 9 22103814 intron variant A/G snv 0.63
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.820 1.000 3 2011 2016
dbSNP: rs646776
rs646776
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.830 1.000 3 2011 2016
dbSNP: rs944797
rs944797
0.882 0.120 9 22115287 intron variant T/C;G snv 0.49
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 3 2011 2013
dbSNP: rs11206510
rs11206510
0.763 0.240 1 55030366 intergenic variant T/A;C;G snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.820 1.000 2 2011 2013
dbSNP: rs1122608
rs1122608
0.763 0.120 19 11052925 intron variant G/T snv 0.18
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.820 1.000 2 2011 2016
dbSNP: rs12524865
rs12524865
1.000 0.040 6 133875536 intron variant C/A snv 0.34
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 2 2011 2012
dbSNP: rs12526453
rs12526453
0.827 0.160 6 12927312 intron variant C/G snv 0.27
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.820 1.000 2 2011 2017
dbSNP: rs1333048
rs1333048
0.683 0.320 9 22125348 intron variant A/C snv 0.44
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 2 2011 2016
dbSNP: rs1412444
rs1412444
0.851 0.120 10 89243170 intron variant C/T snv 0.37
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 2 2011 2011
dbSNP: rs17114046
rs17114046
0.925 0.040 1 56500678 intron variant A/G snv 0.12
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 2 2011 2011
dbSNP: rs1746048
rs1746048
0.776 0.120 10 44280376 downstream gene variant C/T snv 0.25
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.820 1.000 2 2011 2017
dbSNP: rs3798220
rs3798220
LPA
0.732 0.160 6 160540105 missense variant T/C snv 5.6E-02 3.1E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.820 1.000 2 2011 2013
dbSNP: rs4773144
rs4773144
0.827 0.080 13 110308365 intron variant A/G snv 0.42
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.810 1.000 2 2011 2016
dbSNP: rs651007
rs651007
0.851 0.160 9 133278431 upstream gene variant T/A;C snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 2 2011 2011
dbSNP: rs6511720
rs6511720
0.790 0.120 19 11091630 intron variant G/T snv 0.12
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.720 1.000 2 2011 2016
dbSNP: rs6725887
rs6725887
0.851 0.080 2 202881162 intron variant T/C snv 8.9E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 2 2011 2014
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.830 1.000 2 2011 2018
dbSNP: rs9982601
rs9982601
0.851 0.080 21 34226827 intron variant C/T snv 0.15
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.810 1.000 2 2011 2017
dbSNP: rs1004467
rs1004467
0.790 0.280 10 102834750 non coding transcript exon variant A/G snv 0.15 0.14
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs10218795
rs10218795
HJV
1.000 0.040 1 146018957 intron variant G/A snv 0.15
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs10401969
rs10401969
0.776 0.240 19 19296909 intron variant T/C snv 0.10
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 1 2011 2016
dbSNP: rs10455872
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.830 1.000 1 2011 2018
dbSNP: rs10468017
rs10468017
0.851 0.120 15 58386313 intron variant C/T snv 0.24
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs10503669
rs10503669
0.925 0.080 8 19990179 intergenic variant C/A snv 8.4E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs1051730
rs1051730
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011