Disease: Coronary Artery Disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs12785878
NADSYN1
0.677 0.520 11 71456403 intron variant G/A;T snv 25
rs1282382243
DLEU7-AS1 ; DLEU1 ; DLEU7
0.807 0.120 13 50843630 missense variant G/A snv 8
rs1320702652
MFAP1
0.752 0.160 15 43824536 missense variant G/A snv 4.0E-06 11
rs1333040
CDKN2B-AS1
0.732 0.280 9 22083405 intron variant C/G;T snv 15
rs1351855165
DUOX2
0.882 0.040 15 45111550 synonymous variant G/A snv 3
rs1384889210
APOA1 ; APOA1-AS
0.827 0.040 11 116836193 missense variant C/A snv 5
rs14259
PSMD9
0.724 0.360 12 121915890 missense variant A/C;G snv 4.0E-06; 0.32 19
rs142648132
MTR
0.827 0.160 1 236816521 missense variant G/A;C;T snv 8.4E-04; 2.4E-05 5
rs142677199
ACE
0.882 0.040 17 63479897 missense variant G/A;T snv 3.2E-05 4
rs1433748662
KIDINS220
0.882 0.040 2 8791221 missense variant T/C snv 3
rs1458766475
C1orf112 ; SELE
0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 41
rs1466535
LRP1
0.790 0.160 12 57140687 intron variant G/A;C snv 9
rs1501299
ADIPOQ ; ADIPOQ-AS1
0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs150629733
AGTR1
0.851 0.080 3 148741190 missense variant T/C;G snv 4.0E-06; 8.8E-05 4
rs16139
NPY ; LOC107986777
0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
rs16971436
ZFHX3
0.851 0.080 16 72958864 missense variant T/C;G snv 1.2E-05; 7.1E-02 4
rs17465637
MIA3
0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 11
rs1748195
DOCK7
0.851 0.120 1 62583922 intron variant C/G;T snv 8
rs17757541
BCL2
0.827 0.240 18 63212453 intron variant C/G;T snv 7
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs1799889
SERPINE1
0.649 0.600 7 101126430 upstream gene variant A/G snv 31
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1800449
LOX
0.641 0.400 5 122077513 missense variant C/A;T snv 4.0E-06; 0.17 33
rs1800588
ALDH1A2 ; LIPC
0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 16