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
rs1554888939 0.683 0.640 9 137798823 missense variant G/T snv 58
rs886040971 0.683 0.280 8 115604339 stop gained G/A;T snv 56
rs397507520 0.658 0.520 12 112453279 missense variant G/C;T snv 39