Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3219175 0.807 0.240 19 7668969 upstream gene variant G/A snv 5.0E-02 10
rs3743073 0.807 0.120 15 78617197 intron variant G/T snv 0.61 11
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
rs397517132 0.623 0.280 7 55191846 missense variant A/T snv 48
rs629367 0.776 0.200 11 122146306 intron variant C/A snv 0.88 11
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 62
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs712 0.677 0.360 12 25209618 3 prime UTR variant A/C snv 0.46 24
rs760043106 0.645 0.440 17 7674947 missense variant A/C;G;T snv 32
rs767649 0.695 0.480 21 25572410 intron variant T/A snv 7.5E-02 18
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs920778 0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs931127 0.790 0.160 11 65637829 upstream gene variant G/A snv 0.49 12
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 78
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs1353702185 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79
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
rs3212986 0.620 0.400 19 45409478 stop gained C/A;G;T snv 0.29; 4.3E-06; 4.3E-06 42
rs762846821 0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 57