Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4646903
CYP1A1
0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18 36
rs2808630 0.742 0.240 1 159711078 downstream gene variant C/T snv 0.77 13
rs4975616 0.763 0.320 5 1315545 downstream gene variant G/A snv 0.51 12
rs4635969 0.827 0.160 5 1308437 downstream gene variant G/A;T snv 7
rs2746150 0.851 0.240 6 29474924 downstream gene variant C/T snv 5.3E-02 4
rs7459185 0.851 0.160 7 76305323 downstream gene variant G/C;T snv 4
rs10853100
LOC105371808
0.882 0.080 17 48525070 downstream gene variant T/C snv 0.41 3
rs1709084
CYP2A13
0.882 0.080 19 41096565 downstream gene variant A/G snv 0.12 3
rs7248167 0.882 0.080 19 43455962 downstream gene variant A/C snv 0.22 3
rs7452888 0.882 0.080 6 169296169 downstream gene variant A/G snv 0.57 3
rs2256543
HLA-A
0.925 0.080 6 29970056 downstream gene variant T/C snv 0.59 2
rs12167333
HORMAD2
1.000 0.080 22 30179823 downstream gene variant C/T snv 0.21 1
rs1655902
HLA-A
1.000 0.080 6 29949078 downstream gene variant G/A;C snv 1
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
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
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 47
rs1799964
LTA ; LOC100287329 ; TNF
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 47
rs833061
VEGFA
0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
rs1800625
AGER ; PBX2
0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs3834129
CASP8
0.627 0.560 2 201232809 upstream gene variant AGTAAG/- del 0.48 38
rs2853669
TERT
0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 35
rs1800624
PBX2 ; AGER
0.658 0.480 6 32184610 upstream gene variant A/G;T snv 33