Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs2569190 0.620 0.560 5 140633331 intron variant A/G snv 0.57 39
rs10767664 0.752 0.400 11 27704439 intron variant T/A snv 0.83 16
rs7216389 0.732 0.440 17 39913696 intron variant C/T snv 0.60 14
rs10774625 0.763 0.320 12 111472415 intron variant A/G snv 0.66 13
rs2855812 0.790 0.360 6 31504943 intron variant G/T snv 0.23 13
rs4969170 0.752 0.440 17 78364457 intron variant A/C;G snv 0.54 11
rs8076131 0.790 0.200 17 39924659 intron variant G/A;C snv 11
rs4845604 0.776 0.200 1 151829204 intron variant G/A;C;T snv 10
rs2290400 0.790 0.360 17 39909987 intron variant T/C snv 0.48 9
rs4794820 0.790 0.160 17 39933091 intron variant A/G;T snv 9
rs9303277 0.790 0.240 17 39820216 intron variant C/T snv 0.52 9
rs17622378 0.790 0.200 5 132442760 intron variant A/G snv 0.28 8
rs34290285 0.851 0.120 2 241759225 intron variant G/A snv 0.27 8
rs56062135 0.790 0.200 15 67163292 intron variant C/T snv 0.18 8
rs9272346 0.790 0.320 6 32636595 intron variant G/A snv 0.54 8
rs4065275 0.807 0.160 17 39924612 intron variant A/G;T snv 0.56 6
rs4795405 0.851 0.160 17 39932164 intron variant T/A;C snv 6
rs72743461 0.827 0.160 15 67149412 intron variant C/A;T snv 6
rs10445308 0.851 0.240 17 39781794 intron variant C/T snv 0.38 5
rs16917204 0.827 0.160 11 27646808 intron variant G/C snv 0.17 5
rs2428494 0.827 0.160 6 31354420 intron variant T/A;C snv 5
rs2853209 0.827 0.200 20 3670825 intron variant T/A snv 0.41 5