Disease: Ischemic stroke
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12563308
ANGPTL3 ; DOCK7
0.925 0.080 1 62604040 missense variant T/A;C snv 1.9E-02 2
rs174601
FADS2
0.925 0.080 11 61855668 non coding transcript exon variant C/A;T snv 12
rs2188971
ZNF208
0.925 0.080 19 21969380 3 prime UTR variant T/A;C snv 2
rs464218
SORT1
0.925 0.080 1 109313684 3 prime UTR variant G/A snv 0.43 2
rs6698443
PADI4
0.925 0.080 1 17332069 intron variant C/A;T snv 5.2E-02 2
rs6698843
CELSR2
0.925 0.080 1 109264212 synonymous variant C/A;T snv 4.0E-06; 0.44 5
rs9515201
COL4A2
0.925 0.080 13 110388451 intron variant A/C snv 0.63 3
rs978906
ROCK2
0.925 0.080 2 11183150 3 prime UTR variant T/A;C snv 3
rs11634042
ADAMTS7 ; MORF4L1
0.882 0.120 15 78813008 intron variant C/T snv 0.33 4
rs2259820
HNF1A
0.882 0.160 12 120997539 synonymous variant C/T snv 0.34 0.26 6
rs2619112
ALOX15
0.882 0.160 17 4632090 intron variant A/C;G snv 4.0E-06; 0.53 3
rs7395662 0.882 0.080 11 48497341 downstream gene variant A/G snv 0.56 5
rs764522
TGFBR2 ; LOC105377015
0.882 0.080 3 30605058 upstream gene variant G/A;C snv 3
rs767587977
APOB
0.882 0.120 2 21002962 stop gained C/A;T snv 8.2E-06 3
rs17114036
PLPP3
0.851 0.120 1 56497149 intron variant A/G snv 0.11 5
rs1748195
DOCK7
0.851 0.120 1 62583922 intron variant C/G;T snv 8
rs2287218
MVK
0.851 0.080 12 109581533 synonymous variant C/T snv 0.16 0.17 4
rs2650000
HNF1A-AS1
0.851 0.200 12 120951159 intron variant A/C snv 0.70 10
rs651821
APOA5
0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 17
rs6782181
MRAS
0.851 0.160 3 138386212 intron variant G/A;C snv 6
rs7173743
MORF4L1
0.851 0.120 15 78849442 intron variant T/C snv 0.45 6
rs7248488
ZNF208
0.851 0.160 19 22005907 intron variant A/C snv 0.59 5
rs9534275
BRCA2
0.851 0.080 13 32366208 intron variant C/A snv 0.52 7
rs9579646
ALOX5AP
0.851 0.160 13 30736442 intron variant G/A;T snv 6
rs10118757
MTAP
0.827 0.120 9 21853340 intron variant A/G snv 0.26 7