Disease: Cerebrovascular accident
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs799165 0.851 0.120 7 73637727 intergenic variant T/A snv 0.13 17
rs1799998
CYP11B2
0.742 0.200 8 142918184 upstream gene variant A/G;T snv 0.38 14
rs2980853 0.851 0.120 8 125466108 upstream gene variant A/C snv 0.43 16
rs765547 0.827 0.160 8 20008763 intergenic variant G/A;C;T snv 18
rs10757274
CDKN2B-AS1
0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs1333048
CDKN2B-AS1
0.683 0.320 9 22125348 intron variant A/C snv 0.44 24
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs2383206
CDKN2B-AS1
0.742 0.320 9 22115027 intron variant A/G snv 0.49 17
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 22
rs7081476
ANKRD26
0.851 0.120 10 26969741 intergenic variant G/C;T snv 7
rs12420422 0.851 0.120 11 123009573 intergenic variant G/A snv 3.4E-02 16
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs7115242
SIK3
0.851 0.120 11 117037567 intron variant A/G;T snv 16
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs9943582
APLNR
0.807 0.120 11 57237593 upstream gene variant T/C snv 0.63 8
rs12310617 0.851 0.120 12 3060327 intergenic variant C/T snv 0.11 16
rs12369179
ZCCHC8
0.851 0.120 12 122479003 intron variant C/T snv 5.9E-02 16
rs12579302
ATP2B1
0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs5443
CDCA3 ; GNB3
0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs4905014
ITPK1
0.851 0.120 14 92945686 intron variant G/A;C snv 16
rs261332
ALDH1A2 ; LIPC-AS1 ; LIPC
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 20
rs247617 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 20
rs7190256
ZFHX3
0.851 0.120 16 72963084 intron variant C/T snv 0.94 16
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100