Disease: Ischemic stroke
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4537545
IL6R
0.790 0.160 1 154446403 intron variant C/T snv 0.48 11
rs4846914
GALNT2
0.925 0.080 1 230159944 intron variant G/A snv 0.45 6
rs4977574
CDKN2B-AS1
0.695 0.520 9 22098575 intron variant A/G;T snv 26
rs514659
ABO
0.882 0.120 9 133266790 intron variant C/A;T snv 10
rs708272
CETP
0.708 0.440 16 56962376 intron variant G/A snv 0.42 0.38 24
rs7120118
NR1H3
0.716 0.360 11 47264739 intron variant T/C snv 0.38 18
rs7173743
MORF4L1
0.851 0.120 15 78849442 intron variant T/C snv 0.45 6
rs7819412
XKR6
0.827 0.120 8 11187652 intron variant G/A;T snv 6
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs909253
LTA ; LOC100287329
0.641 0.600 6 31572536 intron variant A/G;T snv 34
rs9534275
BRCA2
0.851 0.080 13 32366208 intron variant C/A snv 0.52 7
rs9797861
SLC44A2
0.790 0.200 19 10632450 intron variant C/A;G;T snv 9
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 16
rs1648707 0.925 0.080 3 186833922 intergenic variant A/C snv 0.43 3
rs1878406 0.807 0.200 4 147472512 intergenic variant C/A;G;T snv 7
rs2200733 0.752 0.240 4 110789013 intergenic variant C/T snv 0.18 12
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 15
rs864265 0.925 0.080 3 186836503 intergenic variant T/G snv 0.86 4
rs2107595 0.732 0.280 7 19009765 regulatory region variant G/A snv 0.19 15
rs9860747 0.925 0.080 3 186869628 regulatory region variant T/C snv 0.70 2
rs1042031
APOB
0.790 0.200 2 21002881 stop gained C/A;T snv 8.0E-06; 0.15 11
rs752596535
LDLR
0.752 0.200 19 11105407 stop gained C/A;G;T snv 1.6E-05 14
rs1042579
THBD
0.732 0.240 20 23048087 missense variant G/A;T snv 0.19 16
rs1051266
SLC19A1
0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 41
rs1051931
PLA2G7
0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 19