Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs1360780 0.708 0.320 6 35639794 intron variant T/A;C snv 31
rs2251214 0.827 0.040 12 79430071 intron variant A/G;T snv 7
rs3782025 0.882 0.080 11 113936885 intron variant G/A snv 0.55 4
rs79874540 0.925 0.080 2 231123707 stop gained G/A snv 1.5E-03 1.2E-03 4
rs13134663 1.000 0.040 4 108919403 intron variant A/G;T snv 1