Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs3775291 0.602 0.640 4 186082920 missense variant C/G;T snv 1.2E-04; 0.28 51
rs1801274 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 46
rs8192284 0.724 0.720 1 154454494 missense variant A/C;T snv 19
rs10774671 0.732 0.480 12 112919388 splice acceptor variant G/A;C snv 0.67 14
rs2072136 0.851 0.120 12 112961114 synonymous variant G/A;C snv 0.31; 4.0E-06 6
rs6141 0.925 0.080 3 184372478 3 prime UTR variant C/G;T snv 4.0E-06; 0.56 4
rs669260 0.851 0.080 9 32503442 intron variant T/A;C snv 4
rs1131454 0.882 0.040 12 112911065 missense variant G/A;C snv 0.57 3
rs1447043692 0.925 0.040 10 98641918 missense variant C/T snv 2
rs3205166 0.925 0.040 9 32459452 synonymous variant T/A;G snv 0.35 2
rs15895 1.000 0.040 12 113010483 stop lost A/G;T snv 0.75 1
rs371057322 0.925 0.040 2 8793960 missense variant T/C snv 1.4E-05 2
rs750898115 0.882 0.080 4 75787191 missense variant A/G snv 1.0E-05 3.5E-05 4
rs763780 0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs3740360 0.827 0.240 10 94265734 intron variant A/C snv 9.7E-02 8.4E-02 7
rs8177374 0.672 0.520 11 126292948 missense variant C/T snv 0.12 0.11 22
rs12252 0.695 0.240 11 320772 splice region variant A/G snv 0.13 0.13 23
rs6065 0.851 0.280 17 4933086 missense variant C/T snv 9.8E-02 0.13 6
rs1805016 0.882 0.080 16 27363606 missense variant T/G snv 6.4E-02 0.13 3
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs5745568 0.882 0.080 6 33580617 intron variant G/T snv 0.19 4
rs1799964 0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 47
rs1732778 0.882 0.080 12 113019120 upstream gene variant G/A snv 0.22 5