Disease: Atherosclerosis
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17228212
SMAD3
0.807 0.160 15 67166301 intron variant T/C snv 0.21 8
rs569033466
CETP
0.882 0.160 16 56961929 5 prime UTR variant G/A;C;T snv 4.8E-05; 2.4E-05 6
rs12953
PECAM1
0.763 0.200 17 64356203 missense variant C/A;T snv 0.38 9
rs17465637
MIA3
0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 11
rs1878406 0.807 0.200 4 147472512 intergenic variant C/A;G;T snv 7
rs11556924
ZC3HC1
0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 21
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 16
rs17231520
CETP
0.851 0.240 16 56961915 upstream gene variant G/A snv 2.1E-02 9
rs501120 0.763 0.240 10 44258419 downstream gene variant T/C snv 0.24 10
rs587745372
GJA5 ; LOC102723321
0.851 0.240 1 147773383 upstream gene variant T/A snv 2.8E-05 7
rs2167270
LEP
0.724 0.280 7 128241296 5 prime UTR variant G/A snv 0.37 17
rs112735431
RNF213 ; RNF213-AS1
0.683 0.320 17 80385145 missense variant G/A;C snv 2.6E-04; 8.0E-06 24
rs549858786
IL1B
0.790 0.320 2 112836807 5 prime UTR variant T/A snv 10
rs563558831
CYP2B6
0.776 0.320 19 40991226 upstream gene variant T/C snv 7.0E-06 11
rs1535045
CD40
0.742 0.360 20 46119460 intron variant C/A;G;T snv 12
rs1862513
RETN
0.763 0.360 19 7668907 upstream gene variant C/G;T snv 11
rs3939286 0.776 0.360 9 6210099 regulatory region variant T/A;C snv 12
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 27
rs549591993
F7
0.776 0.400 13 113105794 5 prime UTR variant C/A snv 4.0E-04 2.8E-05 12
rs63750953
HBB
0.790 0.400 11 5227097 5 prime UTR variant TT/- delins 7.0E-06 10
rs6136
SELP
0.752 0.440 1 169594713 missense variant T/G snv 8.2E-02 7.5E-02 17
rs17611
C5
0.732 0.480 9 121006922 missense variant C/T snv 0.47 0.36 14
rs2043211
CARD8
0.653 0.480 19 48234449 missense variant A/T snv 0.33 0.29 29
rs72661131
MBL2
0.742 0.480 10 52771739 upstream gene variant A/G snv 7.6E-04 15
rs1256049
ESR2
0.645 0.560 14 64257333 synonymous variant C/T snv 6.7E-02 6.3E-02 32