Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1131454
OAS1
0.882 0.040 12 112911065 missense variant G/A;C snv 0.57 3
rs1285933
CLEC5A ; MGAM
0.925 0.040 7 141927349 intron variant G/A snv 0.54 2
rs1447043692
HPSE2
0.925 0.040 10 98641918 missense variant C/T snv 2
rs3205166
DDX58
0.925 0.040 9 32459452 synonymous variant T/A;G snv 0.35 2
rs371057322
KIDINS220
0.925 0.040 2 8793960 missense variant T/C snv 1.4E-05 2
rs3739319
IDO1
0.925 0.040 8 39927802 intron variant G/A snv 0.40 0.37 2
rs15895
OAS2
1.000 0.040 12 113010483 stop lost A/G;T snv 0.75 1
rs4859584
ART3 ; CXCL10
1.000 0.040 4 76021984 intron variant G/C snv 0.61 0.61 1
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
rs5745568
GGNBP1 ; BAK1
0.882 0.080 6 33580617 intron variant G/T snv 0.19 4
rs6141
THPO
0.925 0.080 3 184372478 3 prime UTR variant C/G;T snv 4.0E-06; 0.56 4
rs669260
DDX58
0.851 0.080 9 32503442 intron variant T/A;C snv 4
rs750898115
USO1
0.882 0.080 4 75787191 missense variant A/G snv 1.0E-05 3.5E-05 4
rs1805016
IL4R
0.882 0.080 16 27363606 missense variant T/G snv 6.4E-02 0.13 3
rs2072136
OAS3
0.851 0.120 12 112961114 synonymous variant G/A;C snv 0.31; 4.0E-06 6
rs2285932
OAS3
0.851 0.120 12 112949145 synonymous variant T/C snv 0.76 0.78 5
rs739496
SH2B3 ; ATXN2
0.790 0.160 12 111449855 3 prime UTR variant A/G snv 0.27 10
rs12252
IFITM3
0.695 0.240 11 320772 splice region variant A/G snv 0.13 0.13 23
rs3740360
PLCE1
0.827 0.240 10 94265734 intron variant A/C snv 9.7E-02 8.4E-02 7
rs3132468
MICB
0.827 0.240 6 31507709 intron variant C/T snv 0.77 5
rs735239
CD209
0.851 0.240 19 7748382 upstream gene variant A/G snv 0.26 5
rs2287886
CD209
0.776 0.280 19 7747650 upstream gene variant A/G;T snv 0.66 9
rs6065
CHRNE ; GP1BA
0.851 0.280 17 4933086 missense variant C/T snv 9.8E-02 0.13 6
rs3765524
PLCE1
0.724 0.320 10 94298541 missense variant C/T snv 0.27 0.31 17