Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28929495 0.807 0.120 7 55174014 missense variant G/A;C;T snv 3
rs7741164 0.882 0.080 6 41525674 intron variant G/A snv 6.6E-02 3
rs10429489 0.925 0.080 9 21787522 intergenic variant G/A snv 0.26 2
rs1200399 0.925 0.080 14 34823979 intron variant C/T snv 0.87 2
rs121913229 0.925 0.080 7 55174785 missense variant G/C snv 4.0E-06 2
rs2293607 0.807 0.200 3 169764547 non coding transcript exon variant T/A;C snv 2
rs397516975 0.925 0.080 17 39724728 inframe insertion -/ATACGTGATGGC delins 2
rs4236709 0.925 0.080 8 32552592 intron variant G/A;T snv 2
rs55768116 0.925 0.080 11 118237616 intron variant C/A snv 0.38 2