Disease: Atherosclerosis
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1490867890
MCL1 ; LOC107985203
0.882 0.080 1 150579475 missense variant G/A;C snv 3
rs1535045
CD40
0.742 0.360 20 46119460 intron variant C/A;G;T snv 12
rs16147
LOC107986777 ; NPY
0.695 0.400 7 24283791 upstream gene variant T/C snv 0.48 18
rs16933090
SOX6
0.790 0.160 11 16434247 5 prime UTR variant C/T snv 0.12 7
rs17228212
SMAD3
0.807 0.160 15 67166301 intron variant T/C snv 0.21 8
rs17231520
CETP
0.851 0.240 16 56961915 upstream gene variant G/A snv 2.1E-02 9
rs1746048 0.776 0.120 10 44280376 downstream gene variant C/T snv 0.25 8
rs1799889
SERPINE1
0.649 0.600 7 101126430 upstream gene variant A/G snv 31
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs1862513
RETN
0.763 0.360 19 7668907 upstream gene variant C/G;T snv 11
rs1867624 0.851 0.080 17 64309731 upstream gene variant C/T snv 0.65 4
rs1878406 0.807 0.200 4 147472512 intergenic variant C/A;G;T snv 7
rs1927911
TLR4
0.658 0.640 9 117707776 intron variant A/G snv 0.62 28
rs198389
NPPB
0.776 0.240 1 11859214 upstream gene variant A/G snv 0.39 10
rs20417
PACERR ; PTGS2
0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs2071746
HMOX1
0.708 0.320 22 35380679 intron variant A/T snv 0.49 18
rs2106261
ZFHX3
0.763 0.160 16 73017721 intron variant C/G;T snv 11
rs2107595 0.732 0.280 7 19009765 regulatory region variant G/A snv 0.19 15
rs212528
ECE1
0.925 0.040 1 21259168 intron variant T/C snv 0.12 3
rs213045
ECE1
0.851 0.120 1 21290752 intron variant G/T snv 0.44 5
rs2144908
LOC105372629 ; HNF4A
0.851 0.120 20 44357077 intron variant G/A snv 0.18 5