Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 55
rs340005 15 60585831 intron variant G/A snv 0.67 3
rs7310409 0.925 0.160 12 120987058 intron variant A/C;G;T snv 3
rs2393791 0.925 0.160 12 120986153 intron variant C/T snv 0.62 2
rs7979473 12 120982457 intron variant A/C;G snv 2