Disease: Coronary Artery Disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2016520
PPARD
0.752 0.320 6 35411001 5 prime UTR variant C/T snv 0.78 16
rs2234693
ESR1
0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs2236242
SERPINA12
0.776 0.280 14 94493715 intron variant T/A snv 0.31 9
rs2237892
KCNQ1
0.790 0.320 11 2818521 intron variant C/T snv 9.2E-02 16
rs223828
CCL17
0.882 0.240 16 57413502 intron variant T/A;C snv 3
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
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
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 18
rs2943650 0.827 0.120 2 226241205 intergenic variant C/T snv 0.58 6
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 62
rs3737787
TSTD1 ; USF1
0.763 0.280 1 161039733 3 prime UTR variant G/A snv 0.21 11
rs3819024
IL17A
0.701 0.560 6 52185988 upstream gene variant A/G snv 0.34 17
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
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs4788102
SH2B1
0.851 0.160 16 28862077 intron variant G/A snv 0.34 6
rs5082
APOA2
0.807 0.160 1 161223893 upstream gene variant G/A snv 0.68 8
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 27
rs6318
HTR2C ; LOC105373313
0.623 0.520 X 114731326 missense variant C/G;T snv 42
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
rs663129 0.882 0.160 18 60171168 intergenic variant G/A snv 0.24 4
rs670
APOA1 ; APOA1-AS
0.763 0.360 11 116837697 5 prime UTR variant C/T snv 0.17 13