Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2381416 1.000 0.080 9 6193455 upstream gene variant C/A snv 0.65 4
rs10455025 1.000 0.080 5 111069301 upstream gene variant A/C snv 0.24 3
rs16903574 0.882 0.120 5 14610200 missense variant C/A;G snv 4.0E-06; 5.6E-02 6
rs1837253 0.790 0.240 5 111066174 upstream gene variant T/C snv 0.72 10
rs2416257 0.882 0.160 5 111099792 intron variant C/G;T snv 5
rs4594881 1.000 0.080 5 35846713 intergenic variant G/T snv 0.28 2
rs1420101 0.827 0.280 2 102341256 synonymous variant C/T snv 0.33 0.35 8
rs34290285 0.851 0.120 2 241759225 intron variant G/A snv 0.27 8
rs9807989 1.000 0.080 2 102354740 intron variant T/C;G snv 0.46 2
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs2814778 0.763 0.360 1 159204893 5 prime UTR variant T/C snv 0.25 24