Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs121434568 0.568 0.560 7 55191822 missense variant T/A;G snv 73
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
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs1222213359 0.574 0.720 6 43770966 missense variant G/A snv 62
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 62
rs1056836 0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs5275 0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
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
rs153109 0.623 0.600 16 28507775 intron variant T/C snv 0.43 37
rs1463038513
APC
0.658 0.440 5 112839511 frameshift variant TAAA/- delins 36
rs920778 0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs397516436 0.641 0.440 17 7674894 stop gained G/A;C snv 34
rs10505477 0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs4759314 0.649 0.440 12 53968051 non coding transcript exon variant G/A snv 0.93 31
rs1800734 0.653 0.400 3 36993455 5 prime UTR variant G/A snv 0.22 30
rs61764370 0.662 0.320 12 25207290 3 prime UTR variant A/C snv 6.2E-02 29
rs1760944 0.672 0.480 14 20454990 non coding transcript exon variant T/C;G snv 26