Disease: Cerebrovascular accident
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799998
CYP11B2
0.742 0.200 8 142918184 upstream gene variant A/G;T snv 0.38 14
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs20417
PACERR ; PTGS2
0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs2071559
KDR
0.667 0.680 4 55126199 upstream gene variant A/G snv 0.53 26
rs2071746
HMOX1
0.708 0.320 22 35380679 intron variant A/T snv 0.49 18
rs2107595 0.732 0.280 7 19009765 regulatory region variant G/A snv 0.19 15
rs2234693
ESR1
0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs2383206
CDKN2B-AS1
0.742 0.320 9 22115027 intron variant A/G snv 0.49 17
rs2383207
CDKN2B-AS1
0.695 0.280 9 22115960 intron variant A/G snv 0.64 22
rs3850641
TNFSF4
0.716 0.400 1 173206693 intron variant A/G snv 0.14 17
rs3918242
MMP9
0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 54
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs4845625
IL6R
0.851 0.080 1 154449591 intron variant T/C snv 0.60 9
rs5275
PTGS2
0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 28
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 27
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs7025417
LOC107987046 ; IL33
0.752 0.280 9 6240084 intron variant T/C;G snv 11
rs7044343
LOC107987046 ; IL33
0.752 0.520 9 6254208 intron variant C/T snv 0.51 13
rs7173743
MORF4L1
0.851 0.120 15 78849442 intron variant T/C snv 0.45 6
rs765798193
PSMD9
0.732 0.320 12 121915884 frameshift variant G/-;GG delins 18
rs7692387
GUCY1A1
0.925 0.080 4 155714157 intron variant G/A snv 0.16 5