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
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
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs104893877 0.614 0.360 4 89828149 missense variant C/T snv 59
rs10069690 0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs121913499 0.605 0.520 2 208248389 missense variant G/A;C;T snv 51
rs833061 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
rs1800925 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 37
rs78378222 0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03 37
rs1444669684 0.658 0.480 9 21994285 missense variant C/A;T snv 36
rs2853669 0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 35
rs1982073 0.649 0.640 19 41353016 missense variant G/A;C snv 32
rs760043106 0.645 0.440 17 7674947 missense variant A/C;G;T snv 32
rs1800734 0.653 0.400 3 36993455 5 prime UTR variant G/A snv 0.22 30
rs1057519903 0.683 0.080 1 226064434 missense variant A/T snv 28
rs121912660 0.683 0.240 17 7673781 missense variant C/A;G;T snv 26
rs121909218 0.672 0.360 10 87933145 missense variant G/A snv 25
rs121918464 0.708 0.440 12 112450406 missense variant G/A;C snv 25
rs4977756 0.683 0.440 9 22068653 intron variant G/A snv 0.64 24
rs121913503 0.689 0.200 15 90088606 missense variant C/A;T snv 23
rs6010620 0.701 0.360 20 63678486 intron variant A/C;G snv 21
rs121913444 0.724 0.160 7 55191831 missense variant T/A;C;G snv 18