Disease: Ischemic stroke
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10435816
IL33
1.000 0.080 9 6225535 intron variant A/G snv 0.35 2
rs1052053
PMF1 ; PMF1-BGLAP
1.000 0.080 1 156232382 missense variant A/C;G snv 1.0E-03; 0.38 3
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
rs11237379
NDUFC2-KCTD14 ; NDUFC2
1.000 0.080 11 78074911 intron variant T/C snv 0.38 2
rs11957829
LOC100505841
1.000 0.080 5 122179500 intron variant A/G snv 0.18 0.19 2
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
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
rs1263282981
STX17-AS1 ; NR4A3
1.000 0.080 9 99828749 missense variant C/T snv 1.4E-05 2
rs1346452438
LY6G5B ; CSNK2B
1.000 0.080 6 31670987 missense variant G/A snv 2
rs1406885199
HPS1
1.000 0.080 10 98433988 missense variant C/A;T snv 6.0E-06 2
rs147270785
MASP2
1.000 0.080 1 11046616 missense variant G/A snv 6.5E-04 6.4E-04 2
rs152312
PDE4D ; PART1
0.925 0.080 5 60491989 non coding transcript exon variant G/A;T snv 3
rs17222919
ALOX5AP
1.000 0.080 13 30734192 intron variant T/A;G snv 2
rs1804689
HPS1 ; LOC101927278
1.000 0.080 10 98445350 5 prime UTR variant G/T snv 0.28 2
rs2005108 1.000 0.080 11 102899623 downstream gene variant C/G;T snv 3
rs2139733
NOS1
0.925 0.080 12 117288937 intron variant T/A snv 0.39 3
rs2229383
ILF3
1.000 0.080 19 10683954 synonymous variant G/A;C;T snv 4.0E-06; 0.68 2
rs2230500
PRKCH
0.925 0.080 14 61457521 missense variant G/A snv 3.1E-02 1.6E-02 5