Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1946518 0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs113624356 0.724 0.400 11 66526181 missense variant T/G snv 1.5E-03 2.1E-03 22
rs3126184 0.925 0.080 14 49905817 upstream gene variant T/C snv 0.87 2
rs835576 0.925 0.080 1 119912963 3 prime UTR variant T/C snv 0.18 2
rs11101722 1.000 0.080 10 133376925 upstream gene variant T/C snv 8.0E-03 1
rs549908 0.752 0.440 11 112150193 synonymous variant T/A;G snv 4.2E-06; 0.29 10
rs2292832 0.605 0.640 2 240456086 non coding transcript exon variant T/A;C snv 0.59 46
rs952178 1.000 0.080 4 187604743 intron variant T/A;C snv 1
rs755622 0.611 0.720 22 23894205 intron variant G/C snv 0.26 44
rs9612574 1.000 0.080 22 20656929 upstream gene variant G/C snv 8.6E-02 1
rs10509906 0.925 0.080 10 109997916 intron variant G/A;C snv 2
rs1799969 0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 38
rs17139085 1.000 0.080 16 6000072 intron variant G/A snv 6.2E-02 1
rs3755256 1.000 0.080 2 10426288 3 prime UTR variant G/A snv 0.19 1
rs6843588 1.000 0.080 4 168978809 intron variant G/A snv 0.49 1
rs3025039 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs13198304 0.882 0.120 6 6356249 intron variant C/T snv 0.11 3
rs17095355 0.925 0.080 10 109975992 intron variant C/T snv 0.22 2
rs2510389 1.000 0.080 11 68640536 intergenic variant C/T snv 0.15 1
rs4869544 1.000 0.080 5 37700414 non coding transcript exon variant C/T snv 0.70 1
rs3828336 0.925 0.080 2 240451099 non coding transcript exon variant C/G;T snv 0.26 2
rs916145 0.925 0.080 19 35276981 non coding transcript exon variant C/G;T snv 2
rs187238 0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs7251432 0.925 0.080 19 35284538 non coding transcript exon variant A/G;T snv 0.43 2
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105