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
rs1387153 0.807 0.200 11 92940662 downstream gene variant C/G;T snv 10
rs5015480 0.851 0.120 10 92705802 downstream gene variant C/T snv 0.42 9
rs460976 0.851 0.120 21 41463567 downstream gene variant A/G;T snv 7
rs7968585
LINC02354
0.851 0.160 12 47838310 downstream gene variant C/G;T snv 7
rs10509291 0.827 0.280 10 67875446 downstream gene variant T/A snv 7.1E-02 6
rs2383208 0.882 0.120 9 22132077 downstream gene variant A/G;T snv 0.18 5
rs7910977 0.882 0.160 10 92450119 downstream gene variant C/T snv 0.17 4
rs9402571 0.882 0.080 6 134167822 downstream gene variant T/G snv 0.22 4
rs10084572
LOC105372829
1.000 0.040 21 43992991 downstream gene variant T/A;C;G snv 3
rs3132374 1.000 0.040 6 28900717 downstream gene variant C/G snv 5.3E-02 3
rs6583813 0.925 0.080 10 92450182 downstream gene variant C/A;T snv 3
rs1744
HLA-DQA2
1.000 0.040 6 32747257 downstream gene variant A/T snv 1.2E-02 2
rs6502618
TOM1L2
1.000 0.040 17 17843427 downstream gene variant A/G snv 0.55 2
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs25531
SLC6A4 ; LOC105371720
0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs699947
VEGFA
0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs1800587
IL1A
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32 43
rs1570360
VEGFA
0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38
rs266729
ADIPOQ
0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37