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
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
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs763780 0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs1801274 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 46
rs3775291 0.602 0.640 4 186082920 missense variant C/G;T snv 1.2E-04; 0.28 51
rs1143627 0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47
rs1799964 0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 47
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
rs8192284 0.724 0.720 1 154454494 missense variant A/C;T snv 19
rs3765524 0.724 0.320 10 94298541 missense variant C/T snv 0.27 0.31 17
rs4804803 0.732 0.360 19 7747847 upstream gene variant A/G snv 0.26 15
rs10774671 0.732 0.480 12 112919388 splice acceptor variant G/A;C snv 0.67 14
rs2287886 0.776 0.280 19 7747650 upstream gene variant A/G;T snv 0.66 9
rs739496 0.790 0.160 12 111449855 3 prime UTR variant A/G snv 0.27 10
rs3740360 0.827 0.240 10 94265734 intron variant A/C snv 9.7E-02 8.4E-02 7
rs3132468 0.827 0.240 6 31507709 intron variant C/T snv 0.77 5
rs2072136 0.851 0.120 12 112961114 synonymous variant G/A;C snv 0.31; 4.0E-06 6
rs6065 0.851 0.280 17 4933086 missense variant C/T snv 9.8E-02 0.13 6
rs2285932 0.851 0.120 12 112949145 synonymous variant T/C snv 0.76 0.78 5
rs735239 0.851 0.240 19 7748382 upstream gene variant A/G snv 0.26 5
rs669260 0.851 0.080 9 32503442 intron variant T/A;C snv 4