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 34
rs75757892 6 7232156 intron variant C/T snv 0.12 3
rs115024193 4 78793500 intron variant T/A snv 2.3E-02 2