Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs133049 0.882 0.080 22 40635351 intron variant A/- delins 0.82 4
rs35068180 0.851 0.040 11 102845217 upstream gene variant A/-;AA delins 5
rs1333048 0.683 0.320 9 22125348 intron variant A/C snv 0.44 24
rs12032672 0.925 0.040 1 88159953 intron variant A/C snv 0.37 3
rs2229092 1.000 0.040 6 31572980 missense variant A/C snv 4.7E-02 4.2E-02 1
rs1801274 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 46
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs396991 0.742 0.480 1 161544752 missense variant A/C;G;T snv 0.33; 4.1E-06 14
rs13145041 0.925 0.040 4 189616909 intergenic variant A/C;G;T snv 2
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1801275 0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36 58
rs2569190 0.620 0.560 5 140633331 intron variant A/G snv 0.57 39
rs1927911 0.658 0.640 9 117707776 intron variant A/G snv 0.62 28
rs148704956 0.716 0.360 6 52187772 missense variant A/G snv 8.0E-06 7.0E-06 19
rs1131498 0.732 0.360 1 169707345 missense variant A/G snv 0.21 0.22 13
rs30461 0.827 0.120 19 39298475 missense variant A/G snv 0.13 0.25 5
rs1523128 0.882 0.080 3 119781817 5 prime UTR variant A/G snv 0.89 3
rs1932040 0.925 0.040 6 45729051 TF binding site variant A/G snv 0.69 2
rs2723183 1.000 0.040 2 112917144 missense variant A/G snv 6.8E-02 1.0E-01 2
rs4284742 0.925 0.040 19 51628480 intron variant A/G snv 0.78 2
rs6885116 0.925 0.040 5 168216540 intron variant A/G snv 0.14 2