Disease: Ischemic stroke
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1764391
SMIM12 ; GJA4 ; LOC105378642
0.790 0.160 1 34795168 missense variant C/G;T snv 0.30 7
rs1878406 0.807 0.200 4 147472512 intergenic variant C/A;G;T snv 7
rs2228315
SELPLG
0.807 0.120 12 108624122 missense variant C/T snv 0.11 0.14 7
rs9534275
BRCA2
0.851 0.080 13 32366208 intron variant C/A snv 0.52 7
rs1048990
PSMA6
0.790 0.280 14 35292469 5 prime UTR variant C/G;T snv 0.19; 4.0E-06 8
rs16996148 0.882 0.120 19 19547663 downstream gene variant G/T snv 0.10 8
rs1746048 0.776 0.120 10 44280376 downstream gene variant C/T snv 0.25 8
rs440446
APOE
0.807 0.200 19 44905910 missense variant C/G;T snv 0.60 8
rs532019808
NOX4
0.827 0.120 11 89451807 missense variant G/A;C snv 4.0E-06; 4.0E-06 8
rs1049255
CYBA
0.776 0.320 16 88643329 3 prime UTR variant C/T snv 0.49 0.48 9
rs2576178
RNLS ; LIPJ
0.790 0.160 10 88583641 5 prime UTR variant A/G snv 0.29 9
rs544456198
LDLR
0.790 0.120 19 11116930 missense variant G/T snv 8.0E-06 2.8E-05 9
rs6882076
TIMD4
0.827 0.160 5 156963286 upstream gene variant T/C snv 0.56 9
rs9797861
SLC44A2
0.790 0.200 19 10632450 intron variant C/A;G;T snv 9
rs2650000
HNF1A-AS1
0.851 0.200 12 120951159 intron variant A/C snv 0.70 10
rs3774261
ADIPOQ ; ADIPOQ-AS1
0.776 0.320 3 186853770 splice region variant A/G snv 0.55 10
rs3825807
ADAMTS7
0.807 0.120 15 78796769 missense variant A/G snv 0.34 0.33 10
rs41507953
EPHX2
0.790 0.280 8 27500988 missense variant A/G snv 8.7E-02 0.13 10
rs501120 0.763 0.240 10 44258419 downstream gene variant T/C snv 0.24 10
rs514659
ABO
0.882 0.120 9 133266790 intron variant C/A;T snv 10
rs1042031
APOB
0.790 0.200 2 21002881 stop gained C/A;T snv 8.0E-06; 0.15 11
rs147377392
THBD
0.763 0.120 20 23048144 missense variant A/G snv 1.0E-04 2.8E-04 11
rs4537545
IL6R
0.790 0.160 1 154446403 intron variant C/T snv 0.48 11
rs5888
SCARB1
0.752 0.200 12 124800202 synonymous variant A/G;T snv 0.59; 4.0E-06 11
rs2200733 0.752 0.240 4 110789013 intergenic variant C/T snv 0.18 12