Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10069690 0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs10505477 0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs1056836 0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs1057519847 0.570 0.560 7 55191821 missense variant CT/AG mnv 72
rs1057519848 0.570 0.560 7 55191822 missense variant TG/GT mnv 72
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs1131691022 0.827 0.160 17 7670685 frameshift variant GG/A;G delins 6
rs121434568 0.568 0.560 7 55191822 missense variant T/A;G snv 73
rs121913286 0.677 0.280 3 179218306 missense variant C/A;G snv 23
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs1222213359 0.574 0.720 6 43770966 missense variant G/A snv 62
rs1321845532 0.851 0.160 17 7670685 frameshift variant GG/A;G delins 4
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs1760944 0.672 0.480 14 20454990 non coding transcript exon variant T/C;G snv 26
rs1799750 0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs1800734 0.653 0.400 3 36993455 5 prime UTR variant G/A snv 0.22 30
rs1899663 0.683 0.280 12 53967210 intron variant C/A snv 0.28 22
rs2107425 0.732 0.280 11 1999845 intron variant C/T snv 16
rs2494938 0.752 0.240 6 40568389 intron variant G/A snv 0.51 11
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs3760396 0.732 0.280 17 34254422 upstream gene variant G/C snv 0.15 13
rs3803662 0.662 0.440 16 52552429 non coding transcript exon variant A/G snv 0.63 25
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4759314 0.649 0.440 12 53968051 non coding transcript exon variant G/A snv 0.93 31
rs5275 0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55