Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10877887 0.701 0.440 12 62603400 non coding transcript exon variant T/C snv 0.42 18
rs10491121 0.882 0.120 17 36102943 upstream gene variant G/A snv 0.32 5
rs1047781 0.790 0.200 19 48703374 missense variant A/T snv 3.6E-02 1.2E-02 9
rs4938723 0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs3741219 0.776 0.280 11 1995389 non coding transcript exon variant A/G snv 0.42 10
rs2839698 0.662 0.520 11 1997623 non coding transcript exon variant G/A snv 0.41 25
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs2070744 0.608 0.680 7 150992991 intron variant C/T snv 0.70 53
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1800624 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 33
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 55
rs11077 0.732 0.320 6 43523209 3 prime UTR variant T/G snv 0.47 14
rs7963551 0.807 0.160 12 912349 3 prime UTR variant T/G snv 0.13 7
rs10814325 0.827 0.200 9 36036597 upstream gene variant T/A;C;G snv 7
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs290481 0.827 0.200 10 113164066 intron variant C/T snv 0.20 8
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 106
rs7628626 0.925 0.120 3 119525574 3 prime UTR variant A/C snv 0.82 2
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 213
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs145204276 0.658 0.320 1 173868254 splice donor variant CAAGG/- delins 8.8E-02 31