Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs368869806 0.614 0.480 9 95485875 splice acceptor variant C/T snv 4.0E-06 7.0E-06 97
rs1564919048 0.732 0.280 10 121520106 missense variant C/A snv 23
rs1554844486 0.827 0.160 10 75024984 frameshift variant GGGT/- del 10
rs1553200431 0.851 0.240 1 102912180 inframe deletion CCTCACCAGATGGGCCAG/- delins 8
rs1554438441 0.882 0.040 7 143342006 frameshift variant -/TC delins 5