Disease: Atherosclerosis
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1883832
CD40
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs2043211
CARD8
0.653 0.480 19 48234449 missense variant A/T snv 0.33 0.29 29
rs2167270
LEP
0.724 0.280 7 128241296 5 prime UTR variant G/A snv 0.37 17
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs3746444
MIR499A ; MIR499B ; MYH7B ; LOC107985393
0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs3939286 0.776 0.360 9 6210099 regulatory region variant T/A;C snv 12
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4986791
TLR4
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs501120 0.763 0.240 10 44258419 downstream gene variant T/C snv 0.24 10
rs5443
CDCA3 ; GNB3
0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs549591993
F7
0.776 0.400 13 113105794 5 prime UTR variant C/A snv 4.0E-04 2.8E-05 12
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
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
rs569033466
CETP
0.882 0.160 16 56961929 5 prime UTR variant G/A;C;T snv 4.8E-05; 2.4E-05 6
rs587745372
GJA5 ; LOC102723321
0.851 0.240 1 147773383 upstream gene variant T/A snv 2.8E-05 7
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 27
rs6136
SELP
0.752 0.440 1 169594713 missense variant T/G snv 8.2E-02 7.5E-02 17
rs63750953
HBB
0.790 0.400 11 5227097 5 prime UTR variant TT/- delins 7.0E-06 10
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs72661131
MBL2
0.742 0.480 10 52771739 upstream gene variant A/G snv 7.6E-04 15
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93