Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 27
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 25
rs2066865
FGG
0.807 0.240 4 154604124 downstream gene variant G/A snv 0.26 10
rs1746048 0.776 0.120 10 44280376 downstream gene variant C/T snv 0.25 8
rs7968585
LINC02354
0.851 0.160 12 47838310 downstream gene variant C/G;T snv 7
rs56131196
APOC1
0.925 0.160 19 44919589 downstream gene variant G/A snv 0.18 6
rs10920501 0.827 0.120 1 190092815 downstream gene variant A/T snv 0.18 5
rs2067853
AGT
0.851 0.160 1 230702512 downstream gene variant G/A snv 0.25 5
rs2274273
DLGAP5
0.882 0.120 14 55147918 downstream gene variant G/A snv 0.40 5
rs1870634 0.851 0.080 10 43985363 downstream gene variant T/G snv 0.59 4
rs17222842 0.882 0.120 13 30765980 downstream gene variant G/A snv 6.1E-02 3
rs11748327 1.000 0.080 5 4029676 downstream gene variant C/T snv 0.21 2
rs230119 1.000 0.080 9 119152945 downstream gene variant C/A;T snv 2
rs3917639 0.925 0.120 1 94527220 downstream gene variant C/T snv 2
rs1008563 1.000 0.080 2 218162165 downstream gene variant G/A snv 0.43 1
rs6048952
CST3
1.000 0.080 20 23626620 downstream gene variant A/G snv 0.27 1
rs7211079 1.000 0.080 17 80133738 downstream gene variant A/G snv 0.29 1
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs699947
VEGFA
0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
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
rs3918242
MMP9
0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 54
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34