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 24
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 16
rs2710323 0.851 0.080 3 52781889 intron variant T/C snv 0.49 0.54 7
rs4130548 1.000 0.040 1 77998184 intron variant T/C snv 0.25 5