Disease: Ischemic stroke
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7173743
MORF4L1
0.851 0.120 15 78849442 intron variant T/C snv 0.45 6
rs7217186
ALOX15
0.827 0.120 17 4636097 intron variant C/T snv 0.45 5
rs767587977
APOB
0.882 0.120 2 21002962 stop gained C/A;T snv 8.2E-06 3
rs7819412
XKR6
0.827 0.120 8 11187652 intron variant G/A;T snv 6
rs9943582
APLNR
0.807 0.120 11 57237593 upstream gene variant T/C snv 0.63 8
rs1126643
ITGA2
0.807 0.160 5 53051539 synonymous variant C/T snv 0.39 0.36 6
rs1169288
HNF1A-AS1 ; HNF1A
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 21
rs2066715
ABCA1
0.807 0.160 9 104825752 missense variant C/T snv 8.2E-02 5.5E-02 7
rs2259820
HNF1A
0.882 0.160 12 120997539 synonymous variant C/T snv 0.34 0.26 6
rs2576178
RNLS ; LIPJ
0.790 0.160 10 88583641 5 prime UTR variant A/G snv 0.29 9
rs2619112
ALOX15
0.882 0.160 17 4632090 intron variant A/C;G snv 4.0E-06; 0.53 3
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 14
rs4537545
IL6R
0.790 0.160 1 154446403 intron variant C/T snv 0.48 11
rs57137919
ABCG1 ; LOC105372814
0.776 0.160 21 42218908 intron variant G/A snv 0.14 9
rs6782181
MRAS
0.851 0.160 3 138386212 intron variant G/A;C snv 6
rs6882076
TIMD4
0.827 0.160 5 156963286 upstream gene variant T/C snv 0.56 9
rs7248488
ZNF208
0.851 0.160 19 22005907 intron variant A/C snv 0.59 5
rs9579646
ALOX5AP
0.851 0.160 13 30736442 intron variant G/A;T snv 6
rs10033464 0.807 0.200 4 110799605 downstream gene variant T/G snv 0.86 8
rs1042031
APOB
0.790 0.200 2 21002881 stop gained C/A;T snv 8.0E-06; 0.15 11
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 16
rs174546
FADS1 ; FADS2
0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28 17
rs1799998
CYP11B2
0.742 0.200 8 142918184 upstream gene variant A/G;T snv 0.38 14
rs1878406 0.807 0.200 4 147472512 intergenic variant C/A;G;T snv 7
rs2650000
HNF1A-AS1
0.851 0.200 12 120951159 intron variant A/C snv 0.70 10