Disease: Cerebrovascular accident
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 18
rs4905014
ITPK1
0.851 0.120 14 92945686 intron variant G/A;C snv 16
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
rs67608943
PCSK9
0.851 0.080 1 55046549 stop gained C/G;T snv 1.9E-04 8
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
rs7173743
MORF4L1
0.851 0.120 15 78849442 intron variant T/C snv 0.45 6
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
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 18
rs799165 0.851 0.120 7 73637727 intergenic variant T/A snv 0.13 17
rs8082812 0.851 0.120 18 8522684 intergenic variant C/A snv 4.6E-02 16
rs10118757
MTAP
0.827 0.120 9 21853340 intron variant A/G snv 0.26 7
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 19
rs247617 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 20
rs3900940
MYH15
0.827 0.040 3 108428881 missense variant T/A;C snv 4.3E-06; 0.24 6
rs532019808
NOX4
0.827 0.120 11 89451807 missense variant G/A;C snv 4.0E-06; 4.0E-06 8
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
rs1010
VAMP8
0.807 0.120 2 85581859 3 prime UTR variant T/C;G snv 7