Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs796052243 0.695 0.520 4 122934574 inframe deletion CAA/- delins 54
rs121918494 0.790 0.160 10 121517363 missense variant G/C snv 25
rs1569301036 0.827 0.240 X 71397354 missense variant C/T snv 17
rs1554110735 0.776 0.200 6 10398693 frameshift variant TT/- delins 13