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: rs1333049
rs1333049
0.614 0.520 9 22125504 intron variant G/C snv 0.41
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.900 1.000 9 2007 2020
dbSNP: rs10757274
rs10757274
0.701 0.320 9 22096056 intron variant A/G snv 0.41
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.900 1.000 1 2008 2016
dbSNP: rs671
rs671
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.900 1.000 1 2010 2020
dbSNP: rs599839
rs599839
0.724 0.360 1 109279544 downstream gene variant G/A;C snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.850 1.000 3 2007 2018
dbSNP: rs4977574
rs4977574
0.695 0.520 9 22098575 intron variant A/G;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.840 1.000 5 2011 2018
dbSNP: rs17465637
rs17465637
0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.840 1.000 3 2007 2013
dbSNP: rs501120
rs501120
0.763 0.240 10 44258419 downstream gene variant T/C snv 0.24
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.840 1.000 3 2007 2012
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: rs2943634
rs2943634
0.763 0.200 2 226203364 intergenic variant A/C;G snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.830 1.000 2 2007 2012
dbSNP: rs6922269
rs6922269
0.807 0.200 6 150931849 intron variant G/A snv 0.35
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.830 1.000 2 2007 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: 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: rs174547
rs174547
0.742 0.240 11 61803311 intron variant T/C snv 0.28
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.830 1.000 1 2011 2019
dbSNP: rs9349379
rs9349379
0.732 0.200 6 12903725 intron variant A/G snv 0.32
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.820 1.000 4 2011 2019
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: 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: 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: 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: rs2259816
rs2259816
0.827 0.280 12 120997784 synonymous variant G/A;T snv 6.7E-06; 0.40
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.820 1.000 2 2009 2011
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: rs12190287
rs12190287
0.708 0.280 6 133893387 3 prime UTR variant C/G;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.820 1.000 1 2011 2017
dbSNP: rs3184504
rs3184504
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.820 1.000 1 2011 2018
dbSNP: rs4420638
rs4420638
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.820 1.000 1 2009 2016
dbSNP: rs7865618
rs7865618
0.776 0.240 9 22031006 non coding transcript exon variant G/A;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.820 1.000 1 2011 2017