Disease: Ischemic stroke
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10937273 0.882 0.160 3 186831906 downstream gene variant G/A snv 0.33 4
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 16
rs1648707 0.925 0.080 3 186833922 intergenic variant A/C snv 0.43 3
rs16996148 0.882 0.120 19 19547663 downstream gene variant G/T snv 0.10 8
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 16
rs1746048 0.776 0.120 10 44280376 downstream gene variant C/T snv 0.25 8
rs1878406 0.807 0.200 4 147472512 intergenic variant C/A;G;T snv 7
rs2107595 0.732 0.280 7 19009765 regulatory region variant G/A snv 0.19 15
rs2200733 0.752 0.240 4 110789013 intergenic variant C/T snv 0.18 12
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 15
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 14
rs501120 0.763 0.240 10 44258419 downstream gene variant T/C snv 0.24 10
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 28
rs651007 0.851 0.160 9 133278431 upstream gene variant T/A;C snv 22
rs7395662 0.882 0.080 11 48497341 downstream gene variant A/G snv 0.56 5
rs864265 0.925 0.080 3 186836503 intergenic variant T/G snv 0.86 4
rs9860747 0.925 0.080 3 186869628 regulatory region variant T/C snv 0.70 2
rs2230806
ABCA1
0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 24
rs2740483
ABCA1 ; LOC105376196
0.882 0.120 9 104928254 intron variant G/C snv 0.75 3
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs514659
ABO
0.882 0.120 9 133266790 intron variant C/A;T snv 10
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs3825807
ADAMTS7
0.807 0.120 15 78796769 missense variant A/G snv 0.34 0.33 10
rs12495941
ADIPOQ
0.851 0.280 3 186850391 intron variant G/T snv 0.35 5