Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs910049 0.776 0.400 6 32347950 intron variant T/C snv 0.76 5
rs3130501 0.851 0.280 6 31168676 intron variant A/G snv 0.78 3
rs7202877 0.882 0.160 16 75213347 intergenic variant T/C;G snv 3
rs3132524 0.925 0.160 6 31168937 intron variant T/C snv 0.78 2
rs7923837 0.882 0.160 10 92722160 intergenic variant G/A;T snv 2