Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs10069690 0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs1799750 0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs2279744 0.605 0.640 12 68808800 intron variant T/G snv 0.31 48
rs401681 0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs920778 0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs10505477 0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs1447295 0.658 0.400 8 127472793 intron variant A/C;T snv 29
rs2853676 0.667 0.560 5 1288432 intron variant T/A;C snv 29
rs12255372 0.667 0.480 10 113049143 intron variant G/A;T snv 28
rs11568820
VDR
0.672 0.480 12 47908762 intron variant C/T snv 0.38 27
rs2298881 0.653 0.400 19 45423658 intron variant C/A;T snv 25
rs3787016 0.677 0.280 19 1090804 intron variant A/G snv 0.78 24
rs4977756 0.683 0.440 9 22068653 intron variant G/A snv 0.64 24
rs6721961 0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 24
rs8034191 0.695 0.440 15 78513681 intron variant T/C snv 0.27 24
rs762551 0.701 0.400 15 74749576 intron variant C/A snv 0.67 23
rs1899663 0.683 0.280 12 53967210 intron variant C/A snv 0.28 22
rs9651118 0.683 0.480 1 11802157 intron variant T/C snv 0.18 20
rs2267437 0.724 0.320 22 41620695 intron variant C/A;G snv 19
rs11196172 0.708 0.200 10 112967084 intron variant G/A snv 0.13 18