Source: GWASDB

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: rs9818870
rs9818870
MRAS
0.807 0.200 3 138403280 3 prime UTR variant C/A;T snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.740 0.600 1 2011 2019
dbSNP: rs11556924
rs11556924
ZC3HC1
0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.840 0.875 1 2013 2019
dbSNP: rs1333049
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.900 0.944 2 2007 2019
dbSNP: rs2048327
rs2048327
SLC22A3
0.851 0.120 6 160442500 intron variant T/C snv 0.28
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.700 1.000 3 2009 2014
dbSNP: rs12190287
rs12190287
TCF21
0.708 0.280 6 133893387 3 prime UTR variant C/G;T snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.720 1.000 2 2013 2017
dbSNP: rs12936587
rs12936587 		0.882 0.080 17 17640408 regulatory region variant G/A snv 0.38
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.800 1.000 2 2013 2018
dbSNP: rs17114036
rs17114036
PLPP3
0.851 0.120 1 56497149 intron variant A/G snv 0.11
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.710 1.000 2 2013 2018
dbSNP: rs1878406
rs1878406 		0.807 0.200 4 147472512 intergenic variant C/A;G;T snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.710 1.000 2 2013 2015
dbSNP: rs264
rs264
LPL
0.882 0.080 8 19955669 intron variant G/A snv 0.14
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.800 1.000 2 2013 2018
dbSNP: rs3184504
rs3184504
ATXN2 ; SH2B3
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.810 1.000 2 2013 2018
dbSNP: rs7173743
rs7173743
MORF4L1
0.851 0.120 15 78849442 intron variant T/C snv 0.45
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.800 1.000 2 2013 2018
dbSNP: rs9326246
rs9326246 		0.925 0.040 11 116741017 intergenic variant C/G snv 0.93
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.700 1.000 2 2013 2014
dbSNP: rs9982601
rs9982601 		0.851 0.080 21 34226827 intron variant C/T snv 0.15
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.700 1.000 2 2013 2014
dbSNP: rs10755578
rs10755578
LPA
0.925 0.040 6 160548706 intron variant C/G snv 0.44 0.42
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.710 1.000 1 2009 2012
dbSNP: rs10757264
rs10757264
CDKN2B-AS1
1.000 0.040 9 22019733 intron variant A/G snv 0.58
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.700 1.000 1 2007 2007
dbSNP: rs10947789
rs10947789
KCNK5
0.925 0.080 6 39207146 intron variant T/C snv 0.18
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.810 1.000 1 2013 2018
dbSNP: rs10965212
rs10965212
CDKN2B-AS1
0.925 0.080 9 22023796 intron variant T/A;C;G snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.700 1.000 1 2007 2007
dbSNP: rs10965215
rs10965215
CDKN2B-AS1
0.882 0.120 9 22029446 missense variant G/A snv 0.55 0.46
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.700 1.000 1 2007 2007
dbSNP: rs10965219
rs10965219
CDKN2B-AS1
0.882 0.080 9 22053688 intron variant A/G snv 0.58
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.700 1.000 1 2007 2007
dbSNP: rs10965228
rs10965228
CDKN2B-AS1
1.000 0.040 9 22082381 intron variant A/G snv 6.5E-02
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.700 1.000 1 2013 2013
dbSNP: rs11057841
rs11057841
SCARB1
1.000 0.040 12 124832197 intron variant C/T snv 0.18
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.700 1.000 1 2013 2013
dbSNP: rs11072794
rs11072794
CHRNB4 ; LOC105370913 ; LOC112268142
1.000 0.040 15 78714240 intron variant T/C snv 0.57
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.700 1.000 1 2013 2013
dbSNP: rs11191447
rs11191447
AS3MT ; BORCS7-ASMT
1.000 0.040 10 102892566 intron variant C/T snv 9.2E-02
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.700 1.000 1 2013 2013
dbSNP: rs1122608
rs1122608
SMARCA4
0.763 0.120 19 11052925 intron variant G/T snv 0.18
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.720 1.000 1 2014 2016
dbSNP: rs11617955
rs11617955
COL4A1
1.000 0.040 13 110165755 intron variant T/A snv 9.3E-02
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.800 1.000 1 2013 2018