Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs1056836 0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs12921862 0.763 0.200 16 331927 intron variant C/A snv 0.18 10
rs153109 0.623 0.600 16 28507775 intron variant T/C snv 0.43 37
rs1799750 0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs2107425 0.732 0.280 11 1999845 intron variant C/T snv 16
rs370681 0.807 0.200 16 342461 intron variant C/T snv 0.48 6
rs3834129 0.627 0.560 2 201232809 upstream gene variant AGTAAG/- del 0.48 38
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4143815 0.689 0.400 9 5468257 3 prime UTR variant G/C snv 0.23 20
rs4758680 0.763 0.320 12 122170805 intron variant T/A;G snv 9
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 62
rs7977932 0.763 0.320 12 122172836 intron variant C/G;T snv 10
rs874945 0.732 0.240 12 53961667 upstream gene variant C/T snv 0.38 14
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs3218536 0.620 0.440 7 152648922 missense variant C/G;T snv 4.0E-06; 6.4E-02 37
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs1046428 0.776 0.200 14 77327940 missense variant T/A;C snv 4.0E-06; 0.81 8
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193