Disease: Coronary Artery Disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1830321
TEX41 ; LOC100505498
0.827 0.080 2 145067988 intron variant C/T snv 0.40 5
rs2292832
MIR149 ; GPC1 ; LOC100130449
0.605 0.640 2 240456086 non coding transcript exon variant T/A;C snv 0.59 46
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 15
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 18
rs371150372
CAD
0.882 0.040 2 27223972 missense variant G/A;T snv 2.8E-05; 4.0E-06 3
rs4251961
IL1RN
0.763 0.200 2 113116890 intron variant T/C snv 0.29 10
rs515135 0.807 0.160 2 21063185 intergenic variant T/C snv 0.73 9
rs6544713
ABCG8
0.925 0.040 2 43846742 non coding transcript exon variant T/C snv 0.75 5
rs6725887
WDR12
0.851 0.080 2 202881162 intron variant T/C snv 8.9E-02 4
rs693
APOB
0.708 0.440 2 21009323 synonymous variant G/A snv 0.39 0.38 24
rs749903604
APOB
0.882 0.080 2 21042450 missense variant G/A snv 8.0E-06 3
rs763172697
CAD
0.882 0.040 2 27233526 missense variant G/T snv 4.0E-06 3
rs767830104
CXCR4
0.752 0.280 2 136115399 missense variant C/G;T snv 4.0E-06; 8.0E-06 13
rs778916575
CAD
0.882 0.040 2 27222595 missense variant G/A snv 1.2E-05 3
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs840616
LOC105373786
0.925 0.040 2 187331742 intron variant T/C snv 0.56 2
rs897876 0.882 0.040 2 65564447 intron variant C/T snv 0.30 4
rs1050450
GPX1
0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 43
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
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
rs17251221
CASR
0.724 0.360 3 122274400 intron variant A/G snv 0.11 18
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121