Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs501120 0.763 0.240 10 44258419 downstream gene variant T/C snv 0.24 10
rs6905288 0.882 0.120 6 43791136 downstream gene variant G/A snv 0.56 9
rs7968585
LINC02354
0.851 0.160 12 47838310 downstream gene variant C/G;T snv 7
rs3093068 1.000 0.040 1 159711574 downstream gene variant G/C snv 0.13 3
rs72801474 5 133108436 downstream gene variant G/A snv 5.2E-02 3
rs1560833 1 153362049 downstream gene variant G/A snv 0.22 2
rs2143678 6 41655295 downstream gene variant G/T snv 0.19 2
rs2569882 6 1619912 downstream gene variant T/C snv 0.50 2
rs4975709
IRX4
5 1877166 downstream gene variant A/C;T snv 2
rs61194703 19 11081517 downstream gene variant A/T snv 0.14 2
rs9330353
PCDH18
4 137518476 downstream gene variant T/A snv 0.55 2
rs10821967
RTKN2
10 62182180 downstream gene variant A/G snv 0.51 1
rs150532297 5 158169198 downstream gene variant G/A snv 4.1E-03 1
rs2246490 14 103517957 downstream gene variant G/T snv 0.67 1
rs4911250 20 32629151 downstream gene variant T/A snv 0.19 1
rs6683021 1 232394844 downstream gene variant A/G snv 0.30 1
rs68085814 17 49058513 downstream gene variant G/A snv 0.28 1
rs740047
LOC105375397
7 92600848 downstream gene variant C/T snv 0.77 1
rs7841408 8 128400582 downstream gene variant A/G snv 0.39 1
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs3918242
MMP9
0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 54
rs1799964
LTA ; LOC100287329 ; TNF
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 47
rs266729
ADIPOQ
0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs7799039
LOC105375494
0.649 0.560 7 128238730 upstream gene variant G/A;C snv 33