Disease: Cerebrovascular accident
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1186757238
PDE4D
1.000 0.040 5 59039089 5 prime UTR variant A/C snv 2
rs145302848
FGFR4
1.000 0.040 5 177093265 synonymous variant C/G snv 2.0E-05 7.0E-05 2
rs3900940
MYH15
0.827 0.040 3 108428881 missense variant T/A;C snv 4.3E-06; 0.24 6
rs5883
CETP
1.000 0.040 16 56973441 synonymous variant C/T snv 5.1E-02 6.6E-02 5
rs11172113
LRP1
0.882 0.080 12 57133500 intron variant T/C snv 0.42 10
rs4845625
IL6R
0.851 0.080 1 154449591 intron variant T/C snv 0.60 9
rs7692387
GUCY1A1
0.925 0.080 4 155714157 intron variant G/A snv 0.16 5
rs1010
VAMP8
0.807 0.120 2 85581859 3 prime UTR variant T/C;G snv 7
rs10118757
MTAP
0.827 0.120 9 21853340 intron variant A/G snv 0.26 7
rs1122608
SMARCA4
0.763 0.120 19 11052925 intron variant G/T snv 0.18 16
rs147377392
THBD
0.763 0.120 20 23048144 missense variant A/G snv 1.0E-04 2.8E-04 11
rs17114036
PLPP3
0.851 0.120 1 56497149 intron variant A/G snv 0.11 5
rs532019808
NOX4
0.827 0.120 11 89451807 missense variant G/A;C snv 4.0E-06; 4.0E-06 8
rs7173743
MORF4L1
0.851 0.120 15 78849442 intron variant T/C snv 0.45 6
rs9943582
APLNR
0.807 0.120 11 57237593 upstream gene variant T/C snv 0.63 8
rs147603016
FGFR4
0.925 0.160 5 177093286 synonymous variant G/A;C snv 1.5E-04; 8.2E-06 3
rs17228212
SMAD3
0.807 0.160 15 67166301 intron variant T/C snv 0.21 8
rs20455
KIF6 ; LOC107986594
0.763 0.160 6 39357302 missense variant A/G snv 0.41 0.49 12
rs2277680
CXCL16
0.776 0.160 17 4735268 missense variant G/A snv 0.47 0.41 10
rs5182
AGTR1
0.742 0.160 3 148741608 synonymous variant C/T snv 0.49 0.41 16
rs775381348
PSMA6
0.807 0.160 14 35308023 missense variant G/T snv 8
rs9579646
ALOX5AP
0.851 0.160 13 30736442 intron variant G/A;T snv 6
rs10033464 0.807 0.200 4 110799605 downstream gene variant T/G snv 0.86 8
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 16
rs1799998
CYP11B2
0.742 0.200 8 142918184 upstream gene variant A/G;T snv 0.38 14