Disease: Ischemic stroke
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs1800470
TGFB1
0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 34
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 28
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 22
rs6136
SELP
0.752 0.440 1 169594713 missense variant T/G snv 8.2E-02 7.5E-02 17
rs670
APOA1 ; APOA1-AS
0.763 0.360 11 116837697 5 prime UTR variant C/T snv 0.17 13
rs2107538
LOC105371744 ; CCL5
0.763 0.360 17 35880776 5 prime UTR variant C/T snv 0.27 11
rs2834167
IL10RB
0.752 0.360 21 33268483 missense variant A/G snv 0.33 0.25 11
rs7950273
PDGFD
0.925 0.120 11 104160870 intron variant C/G snv 0.32 5
rs7535475
LOC105371473
1.000 0.080 1 161493797 intergenic variant C/A;T snv 2