Disease: Cerebrovascular accident
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs261332
ALDH1A2 ; LIPC-AS1 ; LIPC
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 20
rs2866611 0.851 0.120 20 41322165 upstream gene variant A/T snv 0.58 16
rs2980853 0.851 0.120 8 125466108 upstream gene variant A/C snv 0.43 16
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 22
rs460976 0.851 0.120 21 41463567 downstream gene variant A/G;T snv 7
rs4704221
CERT1
0.851 0.120 5 75463358 intron variant T/A;C snv 16
rs4762
AGT
0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 35
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 18
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 22
rs4905014
ITPK1
0.851 0.120 14 92945686 intron variant G/A;C snv 16
rs5370
EDN1
0.630 0.520 6 12296022 missense variant G/T snv 0.23 0.21 37
rs5443
CDCA3 ; GNB3
0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 21
rs5744680
POLK
0.851 0.120 5 75584065 intron variant G/A snv 0.55 18
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 22
rs6533530 0.851 0.120 4 110810780 intergenic variant T/C snv 0.47 16
rs6759518
SLC30A3
0.851 0.120 2 27263727 intron variant G/C snv 5.5E-02 16
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs7081476
ANKRD26
0.851 0.120 10 26969741 intergenic variant G/C;T snv 7
rs7115242
SIK3
0.851 0.120 11 117037567 intron variant A/G;T snv 16
rs7190256
ZFHX3
0.851 0.120 16 72963084 intron variant C/T snv 0.94 16
rs760762
PLCG1
0.851 0.120 20 41147406 intron variant C/A;T snv 0.59 16
rs7632505
SEMA5B
0.827 0.120 3 123019460 intron variant A/G snv 0.34 17
rs765547 0.827 0.160 8 20008763 intergenic variant G/A;C;T snv 18