Disease: Ischemic stroke
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10033464 0.807 0.200 4 110799605 downstream gene variant T/G snv 0.86 8
rs10118757
MTAP
0.827 0.120 9 21853340 intron variant A/G snv 0.26 7
rs10435816
IL33
1.000 0.080 9 6225535 intron variant A/G snv 0.35 2
rs10507391
ALOX5AP
0.776 0.320 13 30737959 intron variant A/T snv 0.52 10
rs10757274
CDKN2B-AS1
0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs10887800
LOC101929727 ; RNLS
0.790 0.280 10 88316086 intron variant A/G;T snv 11
rs10947803
KCNK17
1.000 0.080 6 39302834 intron variant C/A snv 2
rs11196288 1.000 0.080 10 113297684 regulatory region variant A/G snv 5.5E-02 2
rs1122608
SMARCA4
0.763 0.120 19 11052925 intron variant G/T snv 0.18 16
rs11237379
NDUFC2-KCTD14 ; NDUFC2
1.000 0.080 11 78074911 intron variant T/C snv 0.38 2
rs1130864
CRP
0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26 27
rs113092656 0.882 0.120 6 11615072 intergenic variant G/A snv 2.6E-02 5
rs114209171
FUNDC2
0.882 0.120 X 155050522 non coding transcript exon variant T/C snv 0.23 5
rs11833579 0.827 0.200 12 666033 upstream gene variant G/A snv 0.25 6
rs11984041
HDAC9
0.925 0.080 7 18992312 intron variant C/T snv 0.13 3
rs12122341 1.000 0.080 1 115113069 regulatory region variant C/G snv 0.19 2
rs12130333 1.000 0.080 1 62726106 regulatory region variant C/T snv 0.16 4
rs12204590
LOC112267978 ; LINC01394
1.000 0.080 6 1337158 intergenic variant T/A snv 0.14 3
rs12214600
KCNK17
1.000 0.080 6 39300960 intron variant C/T snv 0.14 2
rs12425791 0.882 0.120 12 674318 downstream gene variant G/A;C snv 4
rs12429692
ALOX5AP
1.000 0.080 13 30738041 intron variant A/T snv 0.24 2
rs12445022 1.000 0.080 16 87541726 intergenic variant G/A snv 0.27 2
rs12476527
KCNK3
1.000 0.080 2 26692756 5 prime UTR variant G/C;T snv 3
rs12495941
ADIPOQ
0.851 0.280 3 186850391 intron variant G/T snv 0.35 5