Disease: Cerebrovascular accident
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9349379
PHACTR1
0.732 0.200 6 12903725 intron variant A/G snv 0.32 19
rs9797861
SLC44A2
0.790 0.200 19 10632450 intron variant C/A;G;T snv 9
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs1042579
THBD
0.732 0.240 20 23048087 missense variant G/A;T snv 0.19 16
rs11556924
ZC3HC1
0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 21
rs146292819
ABCA1
0.790 0.240 9 104794495 missense variant T/G snv 2.9E-04 3.8E-04 9
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 18
rs201058276
F7
0.776 0.240 13 113118731 missense variant G/A;C snv 4.8E-05; 4.0E-06 11
rs2288904
SLC44A2
0.807 0.240 19 10631494 missense variant A/G snv 0.80 0.83 8
rs5065
NPPA ; CLCN6 ; NPPA-AS1
0.763 0.240 1 11846011 stop lost A/G snv 0.14 0.21 12
rs10887800
LOC101929727 ; RNLS
0.790 0.280 10 88316086 intron variant A/G;T snv 11
rs11053646
OLR1
0.724 0.280 12 10160849 missense variant C/G snv 0.11 0.13 18
rs12190287
TCF21
0.708 0.280 6 133893387 3 prime UTR variant C/G;T snv 19
rs1333040
CDKN2B-AS1
0.732 0.280 9 22083405 intron variant C/G;T snv 15
rs2107595 0.732 0.280 7 19009765 regulatory region variant G/A snv 0.19 15
rs2108622
CYP4F2
0.742 0.280 19 15879621 missense variant C/T snv 0.27 0.22 20
rs2230806
ABCA1
0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 24
rs2383207
CDKN2B-AS1
0.695 0.280 9 22115960 intron variant A/G snv 0.64 22
rs5063
CLCN6 ; NPPA-AS1 ; NPPA
0.763 0.280 1 11847591 missense variant C/T snv 5.6E-02 5.3E-02 12
rs7025417
LOC107987046 ; IL33
0.752 0.280 9 6240084 intron variant T/C;G snv 11
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs10757274
CDKN2B-AS1
0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs112735431
RNF213 ; RNF213-AS1
0.683 0.320 17 80385145 missense variant G/A;C snv 2.6E-04; 8.0E-06 24
rs1333048
CDKN2B-AS1
0.683 0.320 9 22125348 intron variant A/C snv 0.44 24