Disease: Ischemic stroke
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 16
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
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 14
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
rs651007 0.851 0.160 9 133278431 upstream gene variant T/A;C snv 22
rs651821
APOA5
0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 17
rs1042031
APOB
0.790 0.200 2 21002881 stop gained C/A;T snv 8.0E-06; 0.15 11
rs1042034
APOB
0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78 15
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv 14
rs676210
APOB
0.925 0.120 2 21008652 missense variant G/A;T snv 0.29 12
rs693
APOB
0.708 0.440 2 21009323 synonymous variant G/A snv 0.39 0.38 24
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
rs9534275
BRCA2
0.851 0.080 13 32366208 intron variant C/A snv 0.52 7
rs6698843
CELSR2
0.925 0.080 1 109264212 synonymous variant C/A;T snv 4.0E-06; 0.44 5
rs1748195
DOCK7
0.851 0.120 1 62583922 intron variant C/G;T snv 8
rs174546
FADS1 ; FADS2
0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28 17
rs174601
FADS2
0.925 0.080 11 61855668 non coding transcript exon variant C/A;T snv 12
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs351855
FGFR4
0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 58
rs2650000
HNF1A-AS1
0.851 0.200 12 120951159 intron variant A/C snv 0.70 10
rs1169288
HNF1A-AS1 ; HNF1A
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 21
rs77375493
INSL6 ; JAK2
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187