Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs555607708 0.667 0.360 22 28695869 frameshift variant G/- del 2.0E-03 1.8E-03 33
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 25
rs7931342 0.689 0.360 11 69227030 intergenic variant T/G snv 0.58 19
rs10505477 0.658 0.400 8 127395198 intron variant A/G snv 0.40 13
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 13
rs34612342 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 11
rs7014346 0.732 0.240 8 127412547 intron variant A/G snv 0.63 11
rs138213197 0.701 0.240 17 48728343 missense variant C/T snv 1.8E-03 1.6E-03 8