Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs7977932 0.763 0.320 12 122172836 intron variant C/G;T snv 10
rs77191406 0.790 0.280 6 137881704 3 prime UTR variant C/T snv 7.2E-04 12
rs763059810 0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
rs758272654 0.611 0.680 20 58909201 synonymous variant T/C snv 4.0E-06 7.0E-06 50
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 62
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs3918242 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 54
rs3834129 0.627 0.560 2 201232809 upstream gene variant AGTAAG/- del 0.48 38
rs351855 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 58
rs3212227 0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 65
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 48
rs2295080 0.695 0.320 1 11262571 upstream gene variant G/C;T snv 20
rs2250889 0.667 0.520 20 46013767 missense variant G/C;T snv 0.88; 1.6E-05 24
rs20576 0.637 0.400 8 23200707 missense variant T/G snv 0.15 0.14 34
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs1799864 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs17576 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs13278062 0.807 0.200 8 23225458 non coding transcript exon variant G/A;C;T snv 8