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
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 73
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
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs2279744 0.605 0.640 12 68808800 intron variant T/G snv 0.31 48
rs397517132 0.623 0.280 7 55191846 missense variant A/T snv 48
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46
rs1801157 0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16 46
rs121913273 0.605 0.440 3 179218294 missense variant G/A;C snv 44
rs1800797 0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72 43
rs727503094 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 41
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs1463038513
APC
0.658 0.440 5 112839511 frameshift variant TAAA/- delins 36
rs187084 0.641 0.480 3 52227015 intron variant A/G snv 0.38 36
rs10741657 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34