Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs385893 0.925 0.080 9 4763176 downstream gene variant T/C snv 0.44 9
rs1732778 0.882 0.080 12 113019120 upstream gene variant G/A snv 0.22 5
rs4859584
ART3 ; CXCL10
1.000 0.040 4 76021984 intron variant G/C snv 0.61 0.61 1
rs4804803
CD209
0.732 0.360 19 7747847 upstream gene variant A/G snv 0.26 15
rs2287886
CD209
0.776 0.280 19 7747650 upstream gene variant A/G;T snv 0.66 9
rs735239
CD209
0.851 0.240 19 7748382 upstream gene variant A/G snv 0.26 5
rs6065
CHRNE ; GP1BA
0.851 0.280 17 4933086 missense variant C/T snv 9.8E-02 0.13 6
rs1285933
CLEC5A ; MGAM
0.925 0.040 7 141927349 intron variant G/A snv 0.54 2
rs669260
DDX58
0.851 0.080 9 32503442 intron variant T/A;C snv 4
rs3205166
DDX58
0.925 0.040 9 32459452 synonymous variant T/A;G snv 0.35 2
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 46
rs5745568
GGNBP1 ; BAK1
0.882 0.080 6 33580617 intron variant G/T snv 0.19 4
rs1447043692
HPSE2
0.925 0.040 10 98641918 missense variant C/T snv 2
rs3739319
IDO1
0.925 0.040 8 39927802 intron variant G/A snv 0.40 0.37 2
rs12252
IFITM3
0.695 0.240 11 320772 splice region variant A/G snv 0.13 0.13 23
rs763780
IL17F
0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1143627
IL1B
0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47
rs1805016
IL4R
0.882 0.080 16 27363606 missense variant T/G snv 6.4E-02 0.13 3
rs8192284
IL6R
0.724 0.720 1 154454494 missense variant A/C;T snv 19
rs371057322
KIDINS220
0.925 0.040 2 8793960 missense variant T/C snv 1.4E-05 2
rs1799964
LTA ; LOC100287329 ; TNF
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 47
rs3132468
MICB
0.827 0.240 6 31507709 intron variant C/T snv 0.77 5
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs10774671
OAS1
0.732 0.480 12 112919388 splice acceptor variant G/A;C snv 0.67 14