Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1005230 0.827 0.040 6 43768759 upstream gene variant T/C snv 0.60 5
rs1057519903 0.683 0.080 1 226064434 missense variant A/T snv 28
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs121912660 0.683 0.240 17 7673781 missense variant C/A;G;T snv 26
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs121913499 0.605 0.520 2 208248389 missense variant G/A;C;T snv 51
rs1444669684 0.658 0.480 9 21994285 missense variant C/A;T snv 36
rs1800925 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 37
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs2234248 0.827 0.040 6 41163980 upstream gene variant A/G snv 2.2E-03 5
rs2293157 0.763 0.120 17 42300657 intron variant C/A;T snv 9
rs2297440 0.763 0.080 20 63680946 intron variant T/C snv 0.81 10
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs3024994 0.776 0.120 6 43775770 non coding transcript exon variant C/T snv 3.8E-02 8
rs3092993 0.827 0.040 11 108364388 intron variant C/A snv 0.11 5
rs4295627 0.763 0.200 8 129673211 intron variant T/G snv 0.17 11
rs4977756 0.683 0.440 9 22068653 intron variant G/A snv 0.64 24
rs498872 0.776 0.240 11 118606652 5 prime UTR variant A/G;T snv 10
rs6010620 0.701 0.360 20 63678486 intron variant A/C;G snv 21
rs753152604 0.827 0.040 12 57751680 missense variant C/A snv 7
rs833061 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs1373481065 0.827 0.040 1 67687668 missense variant A/G snv 4.0E-06 6
rs121913500 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 96
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490