Disease: Ischemic stroke
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800449
LOX
0.641 0.400 5 122077513 missense variant C/A;T snv 4.0E-06; 0.17 33
rs1800470
TGFB1
0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs1878406 0.807 0.200 4 147472512 intergenic variant C/A;G;T snv 7
rs20417
PACERR ; PTGS2
0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs2075291
APOA5 ; ZPR1
0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06 15
rs2188971
ZNF208
0.925 0.080 19 21969380 3 prime UTR variant T/A;C snv 2
rs2241766
ADIPOQ ; ADIPOQ-AS1
0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs2292832
MIR149 ; GPC1 ; LOC100130449
0.605 0.640 2 240456086 non coding transcript exon variant T/A;C snv 0.59 46
rs2619112
ALOX15
0.882 0.160 17 4632090 intron variant A/C;G snv 4.0E-06; 0.53 3
rs266729
ADIPOQ
0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs281865545
PECAM1
0.695 0.360 17 64377836 missense variant C/G;T snv 18
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 15
rs3091244
CRP
0.724 0.280 1 159714875 upstream gene variant G/A;T snv 17
rs3135506
APOA5
0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 26
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs4977574
CDKN2B-AS1
0.695 0.520 9 22098575 intron variant A/G;T snv 26
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs5275
PTGS2
0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs532019808
NOX4
0.827 0.120 11 89451807 missense variant G/A;C snv 4.0E-06; 4.0E-06 8
rs5882
CETP
0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 35
rs5888
SCARB1
0.752 0.200 12 124800202 synonymous variant A/G;T snv 0.59; 4.0E-06 11
rs5985
F13A1
0.724 0.280 6 6318562 missense variant C/A;T snv 0.20; 2.4E-05 20
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 27