Disease: Atherosclerosis
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1298417395
COP1
0.882 0.080 1 176206716 missense variant C/T snv 1.4E-05 4
rs1440763451
PPARG
0.882 0.080 3 12416849 missense variant A/G snv 4.0E-06 4
rs4862423
ACSL1
0.882 0.080 4 184805394 intron variant C/T snv 0.37 4
rs755725121
PIK3CD
0.882 0.080 1 9716029 missense variant G/A snv 2.1E-05 7.0E-06 4
rs773297988
PIK3CB
0.882 0.080 3 138698965 missense variant T/C snv 4.0E-06 3.5E-05 4
rs774887459
SGSM3
0.882 0.080 22 40405776 missense variant G/A snv 4.0E-06 4
rs4076317
ANGPTL4
0.882 0.080 19 8364115 intron variant C/G snv 0.25 5
rs3861950
TNFSF4
0.827 0.160 1 173187153 intron variant T/C snv 0.47 7
rs1020608562
CCR5AS ; CCR5
0.807 0.160 3 46373738 missense variant T/C snv 4.0E-06 9
rs4821480
MYH9
0.807 0.160 22 36299201 intron variant G/T snv 0.78 9
rs185847354
ADIPOQ ; ADIPOQ-AS1
0.763 0.160 3 186854460 missense variant T/C snv 3.1E-04 7.0E-05 11
rs1862513
RETN
0.763 0.360 19 7668907 upstream gene variant C/G;T snv 11
rs2106261
ZFHX3
0.763 0.160 16 73017721 intron variant C/G;T snv 11
rs20455
KIF6 ; LOC107986594
0.763 0.160 6 39357302 missense variant A/G snv 0.41 0.49 12
rs1801177
LPL
0.742 0.240 8 19948197 missense variant G/A;C snv 1.4E-02; 2.0E-05 14
rs2536512
SOD3
0.752 0.280 4 24799693 missense variant G/A;T snv 0.55 14
rs5355
C1orf112 ; SELE
0.742 0.240 1 169726729 missense variant G/A snv 4.5E-02 3.3E-02 14
rs118204057
LPL
0.732 0.400 8 19954222 missense variant G/A;C snv 1.9E-04 16
rs2295490
TRIB3
0.724 0.320 20 388261 missense variant A/G;T snv 0.18; 4.0E-06 16
rs3798220
LPA
0.732 0.160 6 160540105 missense variant T/C snv 5.6E-02 3.1E-02 16
rs1022113606
SOD3
0.732 0.280 4 24800161 missense variant G/C snv 1.6E-04 2.1E-05 17
rs1800777
CETP
0.724 0.280 16 56983407 missense variant G/A snv 3.7E-02 2.8E-02 17
rs6136
SELP
0.752 0.440 1 169594713 missense variant T/G snv 8.2E-02 7.5E-02 17
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 18
rs1051931
PLA2G7
0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 19