Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs869312704 0.882 0.160 2 161423752 frameshift variant -/GGCTGCA delins 10
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 8
rs1057519511 1.000 3 9734500 frameshift variant AG/- delins 2
rs1057519522 1.000 10 129877788 stop gained G/A snv 2
rs1555349214 14 36517838 frameshift variant G/- delins 2
rs267606827 0.925 0.120 14 28768203 stop gained G/A snv 1
rs387906726 0.925 0.040 X 15321727 stop gained G/A snv 1
rs145606134 0.882 0.240 X 102937494 missense variant A/G snv 5.4E-03 4.1E-03 1
rs17070145 0.790 0.120 5 168418786 intron variant C/T snv 0.43 1