Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13107325 0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 8
rs1883025 0.807 0.120 9 104902020 intron variant C/T snv 0.28 7
rs9515201 0.925 0.080 13 110388451 intron variant A/C snv 0.63 1
rs2074356 0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 12
rs2278426 1.000 0.080 19 11239812 missense variant C/T snv 0.11 0.11 2
rs11102800 1.000 0.040 1 114498310 intron variant C/T snv 0.58 1
rs6701231 1 118953038 intron variant C/A;G snv 1
rs984222 1 118961220 intron variant C/A;G snv 1
rs6942652 7 121249218 intron variant G/C;T snv 1
rs7776725 1.000 0.080 7 121393067 intron variant T/C snv 0.28 2
rs12110693 6 121837124 intergenic variant G/A snv 0.23 1
rs10808546 8 125483576 intron variant C/T snv 0.39 4
rs11154370 6 126846446 intron variant A/G;T snv 1
rs987763 6 126960402 intron variant C/A;T snv 1
rs1034207 6 127016554 intron variant C/A;G;T snv 0.94 1
rs4580892 6 127088737 intron variant C/T snv 0.32 1
rs9491696 6 127131494 intron variant C/G snv 0.45 1
rs7745274 6 127188012 intron variant G/A snv 0.56 1
rs620861 0.925 0.080 8 127323428 intron variant G/A snv 0.36 1
rs10894604 11 132771851 non coding transcript exon variant T/G snv 0.26 1
rs645040 3 136207780 upstream gene variant G/T snv 0.77 1
rs605066 6 139508529 intron variant C/T snv 0.53 4
rs634869 6 139510620 intron variant T/A;C snv 2
rs900400 0.925 0.080 3 157080986 upstream gene variant T/C snv 0.36 1
rs17213965 16 15788110 intron variant C/T snv 0.24 1