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
rs397507520 0.658 0.520 12 112453279 missense variant G/C;T snv 39
rs1563686762 0.790 0.280 8 116847620 inframe deletion GTT/- delins 16
rs875989803 0.827 0.200 X 41343249 stop gained G/T snv 15