Disease: Coronary Artery Disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs10865710
PPARG
0.763 0.360 3 12311699 intron variant C/G snv 0.25 13
rs1130864
CRP
0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26 27
rs12970134 0.790 0.280 18 60217517 intergenic variant G/A snv 0.21 13
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs1501299
ADIPOQ ; ADIPOQ-AS1
0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 16
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs243865
MMP2
0.600 0.640 16 55477894 intron variant C/T snv 0.19 48
rs266729
ADIPOQ
0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 14
rs3772622
AGTR1
0.851 0.080 3 148717966 intron variant T/A;C snv 4
rs3834458
FADS1 ; FADS2
0.807 0.200 11 61827449 intron variant T/- del 0.28 7
rs3918242
MMP9
0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 54
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs4149313
ABCA1
0.763 0.240 9 104824472 missense variant T/C snv 9
rs4640525
HESX1 ; APPL1
0.925 0.080 3 57229366 intron variant G/C snv 0.36 2
rs659366
UCP2
0.724 0.520 11 73983709 non coding transcript exon variant C/T snv 0.40 17
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs6700896
LEPR
0.827 0.160 1 65624099 intron variant C/T snv 0.44 9
rs6982502 0.882 0.080 8 125467120 intron variant C/T snv 0.62 6
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98