Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs34612342 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 32
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4994 0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs9904341 0.695 0.280 17 78214286 5 prime UTR variant G/A;C;T snv 0.38; 4.8E-06 20
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214