Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs548234 0.763 0.360 6 106120159 intron variant C/T snv 0.76 4
rs6568431 0.790 0.320 6 106140931 intron variant A/C snv 0.61 2
rs9372120 0.851 0.280 6 106219660 intron variant T/G snv 0.16 1
rs573775 0.851 0.320 6 106316991 intron variant G/A snv 0.34 1
rs538557 1.000 0.080 6 106236001 intron variant T/C snv 4.3E-02 1
rs3827644 0.925 0.080 6 106237320 intron variant G/C snv 0.15 1
rs6911490 1.000 0.040 6 106074152 intron variant T/C snv 0.86 1