Disease: Coronary Artery Disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs908832
ABCA2
0.851 0.120 9 137018032 missense variant A/C;G snv 0.97 0.96 4
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs505151
PCSK9
0.732 0.360 1 55063514 missense variant G/A snv 0.95 0.90 18
rs6721961
NFE2L2
0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 24
rs2288904
SLC44A2
0.807 0.240 19 10631494 missense variant A/G snv 0.80 0.83 8
rs10767664
BDNF
0.752 0.400 11 27704439 intron variant T/A snv 0.83 16
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs2227564
PLAU ; C10orf55
0.763 0.320 10 73913343 missense variant T/C snv 0.75 0.81 15
rs1051931
PLA2G7
0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 19
rs428785
ADAMTS1
0.882 0.040 21 26844276 missense variant C/A;G;T snv 1.3E-05; 0.70 0.78 3
rs2016520
PPARD
0.752 0.320 6 35411001 5 prime UTR variant C/T snv 0.78 16
rs180070
LINC01497
0.882 0.040 17 69960745 upstream gene variant G/T snv 0.77 4
rs383830 0.882 0.040 5 100613278 intergenic variant A/T snv 0.76 3
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs3931020 0.882 0.040 1 74769633 downstream gene variant T/C snv 0.71 4
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs7195830
CYBA
0.851 0.080 16 88643304 3 prime UTR variant A/G snv 0.62 0.69 6
rs2010963
VEGFA
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs5082
APOA2
0.807 0.160 1 161223893 upstream gene variant G/A snv 0.68 8
rs565470
COL4A1
0.882 0.040 13 110186299 intron variant A/G snv 0.68 3