Disease: Arteriosclerosis
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2295490
TRIB3
0.724 0.320 20 388261 missense variant A/G;T snv 0.18; 4.0E-06 16
rs243330
SOCS1 ; RMI2 ; LOC105371082
0.851 0.240 16 11257134 intron variant C/T snv 0.49 4
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 18
rs2943650 0.827 0.120 2 226241205 intergenic variant C/T snv 0.58 6
rs3135506
APOA5
0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 26
rs3732378
CX3CR1
0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 48
rs3732379
CX3CR1
0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 38
rs3782886
BRAP
0.724 0.480 12 111672685 synonymous variant T/C snv 1.9E-02 5.9E-03 22
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs4149313
ABCA1
0.763 0.240 9 104824472 missense variant T/C snv 9
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs4961
ADD1
0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 27
rs4994
ADRB3
0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs5351
EDNRB-AS1 ; EDNRB
0.807 0.240 13 77901178 synonymous variant T/C;G snv 0.57 7
rs5370
EDN1
0.630 0.520 6 12296022 missense variant G/T snv 0.23 0.21 37
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
rs5882
CETP
0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 35
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 27
rs660339
UCP2
0.695 0.320 11 73978059 missense variant G/A snv 0.41 0.43 24
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134