Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs4950928
CHI3L1
0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 33
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs2596542
MICA-AS1 ; MICA
0.724 0.200 6 31398818 upstream gene variant C/T snv 0.41 18
rs9275572 0.724 0.360 6 32711222 upstream gene variant A/G;T snv 15
rs2287886
CD209
0.776 0.280 19 7747650 upstream gene variant A/G;T snv 0.66 9
rs10814325
RECK
0.827 0.200 9 36036597 upstream gene variant T/A;C;G snv 7
rs2854116
APOC3
0.807 0.200 11 116829453 upstream gene variant C/T snv 0.51 7
rs2854117
APOC3
0.851 0.200 11 116829426 upstream gene variant T/A;C snv 6
rs4273729 0.851 0.240 6 32710820 upstream gene variant C/A;G;T snv 5
rs12972991 1.000 0.080 19 39241107 upstream gene variant A/C snv 0.19 1
rs12980602 1.000 0.080 19 39262180 upstream gene variant T/C snv 0.25 1
rs4803223 1.000 0.080 19 39255579 upstream gene variant A/G snv 0.13 1
rs6139030
ITPA
1.000 0.080 20 3207087 upstream gene variant T/C snv 8.6E-02 1
rs8109886 1.000 0.080 19 39252122 upstream gene variant C/A snv 0.53 1
rs368234815
IFNL4
0.742 0.280 19 39248514 frameshift variant TT/G;T delins 15
rs1126579
CXCR2
0.776 0.200 2 218136011 3 prime UTR variant T/C snv 0.62 8
rs3921
CXCL10 ; ART3
0.807 0.240 4 76021790 3 prime UTR variant C/G snv 0.61 8
rs4969168
SOCS3
0.790 0.480 17 78357712 3 prime UTR variant A/G snv 0.71 7
rs8878
ART3 ; CXCL10
0.827 0.280 4 76021147 3 prime UTR variant A/C;G snv 5
rs1863918
ADAMTS2
0.882 0.160 5 179112381 3 prime UTR variant G/T snv 0.25 4
rs4803217
IFNL3
0.882 0.120 19 39243580 3 prime UTR variant C/A snv 0.39 4
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35