Disease: Cerebrovascular accident
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4762
AGT
0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 35
rs4704221
CERT1
0.851 0.120 5 75463358 intron variant T/A;C snv 16
rs460976 0.851 0.120 21 41463567 downstream gene variant A/G;T snv 7
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 22
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs2980853 0.851 0.120 8 125466108 upstream gene variant A/C snv 0.43 16
rs2866611 0.851 0.120 20 41322165 upstream gene variant A/T snv 0.58 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
rs2383206
CDKN2B-AS1
0.742 0.320 9 22115027 intron variant A/G snv 0.49 17
rs222826 0.851 0.120 2 146120964 regulatory region variant T/C snv 0.94 16
rs2074755
BAZ1B
0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02 20
rs1869717
MAML3
0.851 0.120 4 139829967 intron variant G/C snv 0.14 16
rs1799998
CYP11B2
0.742 0.200 8 142918184 upstream gene variant A/G;T snv 0.38 14
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 19
rs17140821 0.851 0.120 7 19177581 regulatory region variant G/A snv 7.9E-02 16
rs16867253
GRHL1
0.851 0.120 2 9956965 intron variant G/T snv 5.8E-02 7
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs1333048
CDKN2B-AS1
0.683 0.320 9 22125348 intron variant A/C snv 0.44 24
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv 16
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs12579302
ATP2B1
0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs12420422 0.851 0.120 11 123009573 intergenic variant G/A snv 3.4E-02 16