Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10774671 0.732 0.480 12 112919388 splice acceptor variant G/A;C snv 0.67 14
rs1131454 0.882 0.040 12 112911065 missense variant G/A;C snv 0.57 3
rs1143627 0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47
rs12252 0.695 0.240 11 320772 splice region variant A/G snv 0.13 0.13 23
rs1285933 0.925 0.040 7 141927349 intron variant G/A snv 0.54 2
rs1447043692 0.925 0.040 10 98641918 missense variant C/T snv 2
rs15895 1.000 0.040 12 113010483 stop lost A/G;T snv 0.75 1
rs1732778 0.882 0.080 12 113019120 upstream gene variant G/A snv 0.22 5
rs1799964 0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 47
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1801274 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 46
rs1805016 0.882 0.080 16 27363606 missense variant T/G snv 6.4E-02 0.13 3
rs2072136 0.851 0.120 12 112961114 synonymous variant G/A;C snv 0.31; 4.0E-06 6
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs2285932 0.851 0.120 12 112949145 synonymous variant T/C snv 0.76 0.78 5
rs2287886 0.776 0.280 19 7747650 upstream gene variant A/G;T snv 0.66 9
rs3132468 0.827 0.240 6 31507709 intron variant C/T snv 0.77 5
rs3205166 0.925 0.040 9 32459452 synonymous variant T/A;G snv 0.35 2
rs371057322 0.925 0.040 2 8793960 missense variant T/C snv 1.4E-05 2
rs3739319 0.925 0.040 8 39927802 intron variant G/A snv 0.40 0.37 2
rs3740360 0.827 0.240 10 94265734 intron variant A/C snv 9.7E-02 8.4E-02 7
rs3765524 0.724 0.320 10 94298541 missense variant C/T snv 0.27 0.31 17
rs3775291 0.602 0.640 4 186082920 missense variant C/G;T snv 1.2E-04; 0.28 51